EP1173573A1 - Method for down-regulating il5 activity - Google Patents

Method for down-regulating il5 activity

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Publication number
EP1173573A1
EP1173573A1 EP00920423A EP00920423A EP1173573A1 EP 1173573 A1 EP1173573 A1 EP 1173573A1 EP 00920423 A EP00920423 A EP 00920423A EP 00920423 A EP00920423 A EP 00920423A EP 1173573 A1 EP1173573 A1 EP 1173573A1
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Prior art keywords
polypeptide
cell
nucleic acid
animal
modified
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EP00920423A
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German (de)
English (en)
French (fr)
Inventor
Steen Klysner
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Affitech AS
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Affitech AS
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/52—Cytokines; Lymphokines; Interferons
    • C07K14/54—Interleukins [IL]
    • C07K14/5409—IL-5
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/0005—Vertebrate antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A61K2039/53—DNA (RNA) vaccination
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/55—Fusion polypeptide containing a fusion with a toxin, e.g. diphteria toxin
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention relates to improvements in therapy and prevention of conditions characterized by an elevated level of eosinophil leukocytes, i.e. conditions such as asthma and other chronic allergic diseases. More specifically, the present invention provides a method for down-regulating inter- leukin 5 (IL5) by enabling the production of antibodies against IL5 thereby reducing the level of activity of eosinophils. The invention also provides for methods of producing modified IL5 useful in this method as well as for the modified IL5 as such. Also encompassed by the present invention are nu- cleic acid fragments encoding modified IL5 as well as vectors incorporating these nucleic acid fragments and host cells and cell lines transformed therewith. The invention also provides for a method for the identification of IL5 analogues which are useful in the method of the invention as well as for composi- tions comprising modified IL5 or comprising nucleic acids encoding the IL5 analogues.
  • IL5 inter- leukin 5
  • Asthma is a common disease of the airways, affecting about 10% of the population.
  • the present treatments is primarily based on the administration of steroids and represents a market value exceeding well over a billion dollars.
  • the incidence and morbidity of asthmatics have increased worldwide over the past two decades.
  • Today, an improved understanding of the immunological mechanisms involved in asthmatic conditions combined with an explosive development in biotechnology provides a new basis for the development of alternative and perhaps better strategies for treatment.
  • eosinophils A general feature in the pathogenesis of asthma and other chronic allergic diseases has proven to be elevated numbers of eosinophils, especially in the bronchial mucosa of the lungs. Upon activation eosinophils secrete a number of mediators that are actively involved in the inflammatory airway response. In the activation of eosinophils, interleukin 5 (IL5) plays an important role.
  • IL5 interleukin 5
  • IL5 is a cytokine found in many mammalian species and among others both the human and the murine gene for IL5 have been cloned (Tanabe et al . , 1987, Campbell et al . , 1988).
  • the human gene consists of four exons with three introns positioned at chromosome 5 and codes for a 134 amino acid residue precursor, including a 19 amino acid N-terminal leader sequence which has the amino acid sequence set forth in SEQ ID NO: 62. Posttranslational cleavage generates the mature 115 amino acid residue protein (SEQ ID NO: 1) .
  • the murine IL5 (mIL5) gene similarly codes for a 133 amino acid residue pre-cursor with a 20 amino acid leader sequence which has the amino acid sequence set forth in SEQ ID NO: 64.
  • the processed mature mIL5 is thus 113 amino acid residues long (SEQ ID NO: 12), missing two N-terminal amino acid residues by alignment with human
  • IL5 The amino acid sequences of hIL5 and mIL5 are 70% identical compared to 77% at nucleotide level of the coding regions fAzuma et al . , 1986) . Higher similarity was reported within human primates; 99% identity is reported for the coding regions of the human and the Rhesus monkey nucleotide sequences (Villinger et al . , 1995).
  • the human amino acid sequence has two potential N-glycosyla- tion sites and the murine three.
  • Human IL5 has been shown to be both N-glycosylated as well as O-glycosylated at Thr 3.
  • the active IL5 is a homo-dimer and the 3-dimensional structure of recombinant hIL5 has been determined by X-ray crystallogra- phy (Milburn et al . , 1993) .
  • the 2 monomers are organised in an antiparallel manner and covalently bound by two interchain di- sulfide bridges (44-87' and 87-44')/ thus engaging all 4 cys- teines of the 2 monomers.
  • the secondary structure of the monomers consists of 4 ⁇ - helices (A-D) intermitted by 3 linking regions (loops) including two short stretches of ⁇ -sheets.
  • This 4 ⁇ helix bundle is known as the "common cytokine fold", which has also been reported for IL-2, IL-4, GM-CSF, and M-CSF. But all these are monomers and the homodimer-structure in which the D-helix completes the 4 ⁇ helix motif of the opposite monomer is unique to IL5.
  • the IL5 receptor is primarily present on eosinophils and it is composed of an ⁇ -chain and a ⁇ -chain.
  • the ⁇ -chain of the receptor is specific for IL5 and the ⁇ -chain, which assure high-affinity binding and signal transduction, is shared with the hetero-dimer receptors for IL-3 and GM-CSF.
  • the sharing of a receptor component could be the reason for the cross- competition seen between IL5, IL-3 and GM-CSF (for review, see Lopez et al . , 1992).
  • the C-terminal part of IL5 seems to be important in both bin- ding to the IL5R and for the biological activity, since removal of more than two C-terminal amino acid residues results in a decline in both the binding affinity to the IL5 R and in the biological activity in an IL5 bioassay (Proudfoot et al . , 1996) .
  • Other residues have also been found to be important for binding to the receptor, such as Glul2, which is involved in binding to the ⁇ -chain, while the Arg90 and Glul09 residues are involved in the binding to the ⁇ -chain of the receptor.
  • binding to the IL5R seems to occur in regions overlapping helices A and D, where helix D is primarily responsible for the binding to the specific IL5R ⁇ -chain (Graber et al . , 1995; Takastsu et al . , 1997).
  • the two 4-helix domain motifs seen in the homodimer has strikingly similar secondary and tertiary structure as compared to the cytokine fold found in GM-CSF and M-CSF, IL-2, IL-4 and human and porcine growth hormone (Milburn et al . , 1993).
  • IL-2 IL-2
  • IL-4 human and porcine growth hormone
  • IL5 is mainly secreted by fully differentiated Th2 cells, mast cells and eosinophils (Cousins et al . , 1994; Takutsu et al . , 1997) . It has been shown to act on eosinophils, basophiles, cytotoxic T lymphocytes and on murine B cells (Callard & Gearing, 1994; Takutsu et aJ . , 1997). The effects of IL5 on human B cells are still a matter of controversy. Augmentation of im- munoglobulin synthesis under certain circumstances and binding to a variety of human B cell lines have been demonstrated. Even though mRNA for the hIL5R has been found in human B- cells, the actual presence of the receptor on these cells has still to be verified (Baumann & Paul, 1997; Huston et al . , 1996) .
  • IL5 The actions of IL5 on eosinophils include chemotaxis, enhanced adhesion to endothelial cells, activation and terminal diffe- rentiation of the cells. Furthermore it has been demonstrated that IL5 prevents mature eosinophils from apoptosis (Yamaguchi et al . , 1991). These findings have contributed to the present concept of IL5 as being the most important cytokine for eosi- nophil differentiation (Corrigan & Kay, 1996; Karlen et ai . , 1998) .
  • IL5 and its associated eosinophil activation is considered to serve a protective role against helminthic infections and possibly against certain tumours, since these diseases are typically accompanied by peripheral blood eosinophilia (Takutsu et al . , 1997; Sanderson et al . , 1992). It is, however, somewhat speculative as in two studies the authors failed to show any effect beside eosinophil down- regulation following administration of antibodies against IL5 on the immunity (e.g. IgE levels) against Nippostrongylus braziliensis or Schistosoma mansoni in mice infected with these parasites (Sher et al . , 1990; Coffman et ai . , 1989).
  • a transgenic mouse expressing the IL5 gene in T cells was reported to have an increased white blood cell level characte- rised by expansion of B220+ B lymphocytes and profound eosino- philia. This was accompanied by a massive peritoneal cavity cell exudate dominated by eosinophils and infiltration of eosinophils in nearly all organ systems (Lee et al . , 1997a).
  • Another transgenic mouse expressing the IL5 gene under control of a metallothionin promoter was characterised by an increase in the serum levels of IgM and IgA, a massive eosino- philia in peripheral blood and many other organs accompanied by the expansion of a distinctive CD5+ B cell population, which produce auto-antibodies (Tominaga et ai . , 1991).
  • a third study involved a transgenic mouse constitutively expressing IL5 in the lungs. These animals developed pathophysi- ological changes resembling those of human asthma, including eosinophil invasion of peribronchial spaces, epithelial hypertrophy and increased mucus production. Furthermore, development of airway hyper responsiveness was seen in the absence of antigens (Lee et al . , 1997b) .
  • mice IL5-deficient mice ('knock-out' mice) have also been studied. These mice (C57BL/6) have no obvious signs of disease and are fertile. The immunoglobulin levels and the specific antibody responses to DNP-OVA were normal. Basal levels of eosinophils are produced, but are 2-3 times lower than in control animals, indicating that eosinophils can be produced in the complete absence of IL5. When these mice were infected with Mesoces- toides corti the eosinophilia normally seen was abolished and this absence of eosinophilia did not affect the worm burden produced by this parasite (Kopf et al . , 1996).
  • Asthma affect about 10% of the population worldwide and for yet unknown reasons the incidence and morbidity have increased over the past two decades (Ortega & Busse, 1997) . It is a chronic airway disease characterised by recurrent and usually reversible air flow obstruction, inflammation and hyper responsiveness (Moxam and Costello, 1990) . This produces symptoms of wheezing and breathlessness, which in severe cases can be fatal .
  • Eosinophilia has been identified in bronchoalveolar lavage (BAL) fluid and in bronchial mucosal biopsies of subjects with asthma and correlates with disease severity.
  • BAL bronchoalveolar lavage
  • Several eosinophil products have been identified in the BAL fluid of patients with asthma and numbers of peripheral blood eosinophils correlate with asthma severity (Ortega & Busse 1997) .
  • IL5 serum concentration was found to be elevated (median concentration 150 pg/ml) in 15 out of 29 patients with chronic severe asthma as compared to control subjects (Alexander et al . , 1994) .
  • corticoste- roids which, by their anti-inflammatory action, are the most powerful drugs.
  • ⁇ 2 agonists and methyl xanthine derivatives which all cause bronchodilation, and disodium chromoglycate which 'stabilises' mast cells, thereby preventing mediator release, all have proven beneficial in asthma patients (Ortega & Busse 1997) .
  • antisense IL5 oligonucleotides for antisense therapy has been suggested by the company Hybridon for the treatment of asthma, allergies and inflammation.
  • the antisense technology has proven to be technically difficult and, in fact, conclusive evidence of the feasibility of antisense therapy in humans has not yet been established.
  • WO 97/45448 (Bresagen Limited / Medvet Science) proposes the use of "modified and variant forms of IL5 molecules capable of antagonising the activity of IL5" in ameliorating, abating or otherwise reducing the aberrant effects caused by native or mutant forms of IL5.
  • the antagonizing effect is reported to be the result of the variant forms of IL5 binding to the low affinity ⁇ chain of IL5R but not to the high affinity receptors; in this way the variants compete with IL5 for bin- ding to its receptors without exerting the physiological effects of IL5.
  • Other atopic diseases involving eosinophilic inflammation are treated with either the symptomatica mentioned for asthma or immune therapy (IT) using hyposensitization with allergen extracts.
  • IT immune therapy
  • the latter type of treatment is known to be effective against allergies against one or a few antigens, whereas IT is not feasible in the treatment of multiple allergies.
  • the time scale for obtaining clinical improvement in patients susceptible to treatment is very long
  • the object of the present invention is to provide novel thera- pies against chronic allergic conditions (such as asthma) characterized by eosinophilia.
  • a further object is to develop an autovaccine against IL5, in order to obtain a novel treatment for asthma and for other pathological disorders involving chronic airway inflammation.
  • the T-cell derived cytokine IL5 has, as mentioned above, a crucial role in orchestrating the eosinophilic response, affecting both the production, the localisation and the activation of eosinophils.
  • IL5 has not otherwise been reported to have a central role in the development of a protective immune response, this particular cytokine is in the opinion of the inventors an attractive therapeutic target for the treatment of asthma.
  • the general aim according to the present invention is to decrease the pathogenic levels of eosinophils in the airways of the asthma patient by down-regulating of the IL5 levels, since eosinophils depend on IL5 for attraction and activation.
  • the result of a decreased eosinophil number in the airway mucosa would be a concomitant decrease in the airway inflammation, corresponding to a clinical improvement in the asthmatic patient .
  • This current invention takes the results obtained through passive immunisation one step further by using the approach of generating an active immune response through the concept of autovaccination. To the best of the inventor's knowledge, such an approach has never been suggested before.
  • the effect of an induced polyclonal Ab response is expected to be superior to passively injected monoclonal immunoglobulins since the polyclonal response has a broader specificity. Improvements with respect to administration regimen are also expected (since effective autovaccines described herein typically would require a maximum of 2-6 administrations per year) .
  • the present invention offers the attractive aspect of being non-specific; this is es- pecially relevant when dealing with multi-allergic patients.
  • the present invention relates to a method for in vivo down-regulation of in- terleukin 5 (IL5) activity in an animal, including a human being, the method comprising effecting presentation to the animal's immune system of an immunologically effective amount of at least one IL5 polypeptide or subsequence thereof which has been formulated so that immunization of the animal with the IL5 polypeptide or subsequence thereof induces production of antibodies against the IL5 polypeptide, and/or at least one IL5 analogue wherein is introduced at least one modification in the IL5 amino acid sequence which has as a result that immunization of the animal with the analogue induces production of antibodies against the IL5 polypeptide.
  • IL5 polypeptide an immunologically effective amount of at least one IL5 polypeptide or subsequence thereof which has been formulated so that immunization of the animal with the IL5 polypeptide or subsequence thereof induces production of antibodies against the IL5 polypeptid
  • asthma can be controlled by periodic but not very frequent immunizations, in contrast to a therapeutic approach which involves administration of anti-IL5 or molecules having a binding affinity to IL5 analogous therewith. It is expected that 1-4 annual injections with an immunogenic composition according to the invention will be sufficient to obtain the desired effect, whereas administration of other inhibitors of IL5 activity does or will require daily, or at least weekly, administrations .
  • the invention also relates to IL5 analogues as well as to nucleic acid fragments encoding a subset of these. Also immunogenic compositions comprising the analogues or the nucleic acid fragments are part of the invention.
  • the invention also relates to a method of identifying analogues of IL5 as well as a method for preparing a composition comprising the IL5 analogues.
  • Fig. 1 The amino acid sequence of the mature human IL5
  • the aligned murine sequence is in- eluded (SEQ ID NO: 12), but only positions that differ from the human sequence are displayed.
  • the two "*"s indicate the missing N-terminal residues of the murine IL5.
  • the N-glycosylation positions are marked with double underlining, the O-glycosylated threo- nines of human IL5 are given in italics, and the cysteines in bold.
  • Fig. 2 The dimer and monomer structures of human IL5.
  • A Dimer structure of hIL5. The structure has only been obtained for residues 5-112, which means that the O-glycosylation site at Thr3 is not included.
  • Fig. 3 The aligned mature human IL5 (hIL5) and murine IL5
  • amino acid sequences to be substituted with foreign T H epitope containing peptides are marked in bold; one such sequence is surrounded by a dot-lined box because of residues overlapping with those substituted in a different construct.
  • the amino acid sequences of 10 constructs (5 derived from human and 5 derived from murine IL5) are set forth m SEQ ID NOs: 2-11 and 13-22.
  • Fig. 4 ELISA results of DNA immunization testing two mIL5 autovaccme DNA vaccines .
  • mice were DNA vaccinated with naked plasmid DNA encoding either ovalbumin, mIL5wt, mIL5.1 or mIL5.5. Sera obtained at day 77 were tested for reactivity against ovalbumin and murine IL5. Polystyrene micro- titer plates (Maxisorp, Nunc) were coated with ovalbumin (1 ⁇ g/well, Sigma) or purified recombinant murine IL5 (0.1 ⁇ g/well, E1320). The reactivities of diluted sera added to the wells were visualised using a goat anti-mouse secondary antibody.
  • OD490 readings of the pre-bleeds were subtracted from the OD490 readings of the test samples, and the resulting values were presented for each individual mouse as bars.
  • the OD490 readings of the pre-bleeds (in 1:25 dilution) were ranging from 0.025-0.034.
  • Crucifixes indicate dead animals.
  • Fig. 5 Schematic representation of murine IL5 based autovaccme constructs.
  • the top figure represents murine wild-type IL5 mono- mer with helices A-C, loops 1-3 and the flexible C- ter inal region.
  • Remaining figures represent different autovaccme constructs having m-substitutions of the tetanus toxoid epitopes P2 and P30 in various positions. Specific constructs are detailed in the Examples. DETAILED DISCLOSURE OF THE INVENTION
  • T-lymphocyte and "T-cell” will be used inter- changeably for lymphocytes of thymic origin which are responsible for various cell mediated immune responses as well as for helper activity in the humeral immune response.
  • B-lymphocyte and “B-cell” will be used interchangeably for antibody-producing lymphocytes.
  • IL5 polypeptide is herein intended to denote polypeptides having the amino acid sequence of the above-discussed IL5 proteins derived from humans and mice (or truncates thereof sharing a substantial amount of B-cell epitopes with intact IL5) , but also polypeptides having the amino acid sequence identical to xeno-analogues of these two proteins isolated from other species are embraced by the term. Also unglycosylated forms of IL5 which are prepared in prokaryotic system are included within the boundaries of the term as are forms having varying glycosylation patterns due to the use of e.g. yeasts or other non-mammalian eukaryotic expression systems.
  • an IL5 polypeptide it is intended that the polypeptide in question is normally non-immunogenic when presented to the animal to be treated.
  • the IL5 polypeptide is a self-protein or is a xeno-analogue of such a self-protein which will not normally give rise to an immune response against IL5 of the animal in question.
  • an "IL5 analogue” is an IL5 polypeptide which has been subjected to changes in its primary structure.
  • a change can e.g. be in the form of fusion of an IL5 polypeptide to a suitable fusion partner (i.e. a change in primary structure exclu- sively involving C- and/or N-terminal additions of amino acid residues) and/or it can be in the form of insertions and/or deletions and/or substitutions in the IL5 polypeptide' s amino acid sequence.
  • a suitable fusion partner i.e. a change in primary structure exclu- sively involving C- and/or N-terminal additions of amino acid residues
  • derivatized IL5 molecules cf. the discussion below of modifications of IL5.
  • a vaccine in a human of e.g. a canine analogue of human IL5 can be imagined to produce the desired immunity against IL5.
  • Such use of an xeno-analogue for immunization is also considered to be an "IL5 analogue" as defined above.
  • IL5 When using the abbreviation "IL5" herein, this is intended as a reference to the amino acid sequence of mature, wildtype IL5 (also denoted “IL5m” and “IL5wt” herein) .
  • Mature human IL5 is denoted hIL5, hIL5m or hIL5wt, and murine mature IL5 is denoted mIL5, mIL5m, or mIL5wt.
  • a DNA construct includes information encoding a leader sequence or other mate- rial, this will normally be clear from the context.
  • polypeptide is in the present context intended to mean both short peptides of from 2 to 10 amino acid residues, oligopeptides of from 11 to 100 amino acid residues, and poly- peptides of more than 100 amino acid residues. Furthermore, the term is also intended to include proteins, i . e . functional biomolecules comprising at least one polypeptide; when comprising at least two polypeptides, these may form complexes, be covalently linked, or may be non-covalently linked.
  • the polypeptide (s) in a protein can be glycosylated and/or lipi- dated and/or comprise prosthetic groups.
  • sequence means any consecutive stretch of at least 3 amino acids or, when relevant, of at least 3 nucleo- tides, derived directly from a naturally occurring IL5 amino acid sequence or nucleic acid sequence, respectively.
  • animal is in the present context in general intended to denote an animal species (preferably mammalian) , such as Homo sapi ens, Cani s domesti cus, etc. and not just one single animal. However, the term also denotes a population of such an animal species, since it is important that the individuals immunized according to the method of the invention all harbour substantially the same IL5 allowing for immunization of the animals with the same immunogen (s) .
  • an animal in the present context is a living being which has an immune system. It is preferred that the animal is a vertebrate, such as a mammal.
  • ⁇ in vi vo down-regulation of IL5 activity is herein meant reduction in the living organism of the number of interactions between IL5 and its receptors (or between IL5 and other possible biologically important binding partners for this molecule) .
  • the down-regulation can be obtained by means of several mechanisms: Of these, simple interference with the active site in IL5 by antibody binding is the most simple. However, it is also within the scope of the present invention that the antibody binding results in removal of IL5 by scavenger cells (such as macrophages and other phagocytic cells) .
  • effecting presentation ... to the immune system is intended to denote that the animal's immune system is subjected to an immunogenic challenge in a controlled manner.
  • challenge of the immune system can be effected in a number of ways of which the most important are vaccination with polypeptide containing "pharmaccines” (i.e. a vaccine which is administered to treat or ameliorate ongoing disease) or nucleic acid "pharmaccine” vaccination.
  • pharmaceutical competent cells in the animal are confronted with the antigen in an immunologically effective manner, whereas the precise mode of achieving this result is of less importance to the inventive idea underlying the present invention.
  • immunogenically effective amount has its usual meaning in the art, i.e. an amount of an im unogen which is capable of inducing an immune response which significantly engages pathogenic agents which share immunological features with the immunogen.
  • IL5 When using the expression that the IL5 has been "modified" is herein meant a chemical modification of the polypeptide which constitutes the backbone of IL5.
  • a modification can e.g. be derivatization (e.g. alkylation, acylation, esterification etc.) of certain amino acid residues in the IL5 sequence, but as will be appreciated from the disclosure below, the preferred modifications comprise changes of (or additions to) the primary structure of the IL5 amino acid sequence.
  • IL5 is a self-protein in the population to be vaccinated, normal individuals in the population do not mount an immune response against IL5; it cannot be excluded, though, that occasional individuals in an animal population might be able to produce antibodies against native IL5, e.g. as part of an autoimmune disorder.
  • an animal will normally only be autotolerant towards its own IL5, but it cannot be excluded that IL5 analogues derived from other animal species or from a population having a different IL5 phenotype would also be tolerated by said animal.
  • a “foreign T-cell epitope” is a peptide which is able to bind to an MHC molecule and which stimulates T-cells in an animal species.
  • Preferred foreign T-cell epitopes in the invention are "promiscuous" epitopes, i.e. epitopes which bind to a substantial fraction of a particular class of MHC molecules in an animal species or population. Only a very limited number of such promiscuous T- cell epitopes are known, and they will be discussed in detail below.
  • m order for the immunogens which are used according to the present invention to be effective in as large a fraction of an animal population as possible it may be necessary to 1) insert several foreign T-cell epitopes in the same IL5 analogue or 2) prepare several IL5 analogues wherein each analogue has a different promiscuous epitope inserted.
  • the concept of foreign T-cell epitopes also encompasses use of cryptic T-cell epitopes, i.e. epitopes which are derived from a self-protein and which only exerts immunogenic behaviour when existing in isolated form without being part of the self-protein in question.
  • a "foreign T helper lymphocyte epitope" (a foreign T H epitope) is a foreign T cell epitope which binds an MHC Class II molecule and can be presented on the surface of an antigen presenting cell (APC) bound to the MHC Class II molecule.
  • APC antigen presenting cell
  • a "functional part" of a (bio) molecule is in the present con- text intended to mean the part of the molecule which is responsible for at least one of the biochemical or physiological effects exerted by the molecule. It is well-known in the art that many enzymes and other effector molecules have an active site which is responsible for the effects exerted by the mole- cule in question. Other parts of the molecule may serve a stabilizing or solubility enhancing purpose and can therefore be left out if these purposes are not of relevance in the context of a certain embodiment of the present invention. For instance it is possible to use certain other cytokines as a modifying moiety in IL5 (cf. the detailed discussion below), and in such a case, the issue of stability may be irrelevant since the coupling to IL5 provides the stability necessary.
  • adjuvant has its usual meaning in the art of vac- cine technology, i.e. a substance or a composition of matter which is 1) not in itself capable of mounting a specific immune response against the immunogen of the vaccine, but which is 2) nevertheless capable of enhancing the immune response against the immunogen.
  • vaccination with the adjuvant alone does not provide an immune response against the immunogen
  • vaccination with the immunogen may or may not give rise to an immune response against the immunogen, but the combination of vaccination with immunogen and adjuvant induces an immune response against the immunogen which is stronger than that induced by the immunogen alone.
  • Targeting of a molecule is in the present context intended to denote the situation where a molecule upon introduction in the animal will appear preferentially in certain tissue (s) or will be preferentially associated with certain cells or cell types.
  • the effect can be accomplished in a number of ways including formulation of the molecule in composition facilita- ting targeting or by introduction in the molecule of groups which facilitates targeting.
  • Stimulation of the immune system means that a substance or composition of matter exhibits a general, non-specific immu- nostimulatory effect.
  • a number of adjuvants and putative adjuvants (such as certain cytokines) share the ability to stimulate the immune system.
  • the result of using an immunostimulating agent is an increased "alertness" of the immune system meaning that simultaneous or subsequent immunization with an immunogen induces a significantly more effective immune response compared to isolated use of the immunogen
  • the IL5 polypeptide used as an immunogen in the method of the invention is a modified molecule wherein at least one change is present in the IL5 amino acid sequence, since the chances of obtaining the all-important breaking of autotolerance towards IL5 is greatly facilitated that way. It should be noted that this does not exclude the possibility of using such a modified IL5 in formulations which further facilitate the breaking of autotolerance against IL5, e.g. for- mulations containing certain adjuvants discussed in detail below.
  • T-cells recognizing the foreign element are activated upon recognizing the foreign epitope on an APC (such as, initially, a mononuclear cell) .
  • APC such as, initially, a mononuclear cell
  • Polyclonal B-lymphocytes capable of recognising self-epitopes on the modified self-protein also internalise the antigen and subsequently presents the foreign T-cell epitope (s) thereof, and the activated T-lymphocytes subsequently provide cytokine help to these self-reactive polyclonal B-lymphocytes.
  • the antibodies produced by these polyclonal B- lymphocytes are reactive with different epitopes on the modified polypeptide, including those which are also present in the native polypeptide, an antibody cross-reactive with the non-modified self-protein is induced.
  • the T-lymphocytes can be led to act as if the population of poly- clonal B-lymphocytes have recognised an entirely foreign antigen, whereas in fact only the inserted epitope (s) is/are foreign to the host. In this way, antibodies capable of cross-reacting with non-modified self-antigens are induced.
  • the modification can include that at least one foreign T-cell epitope is introduced, and/or at least one first moiety is introduced which effects targeting of the modified molecule to an antigen presenting cell (APC) , and/or - at least one second moiety is introduced which stimulates the immune system, and/or at least one third moiety is introduced which optimises presentation of the modified IL5 polypeptide to the immune system.
  • APC antigen presenting cell
  • side groups in the form of foreign T-cell epitopes or the above-mentioned first, second and third moieties
  • side groups are covalently or non-covalently introduced. This is intended to mean that stretches of amino acid residues derived from IL5 are derivatized without altering the primary amino acid sequence, or at least without introducing changes in the peptide bonds between the individual amino acids in the chain.
  • An alternative, and preferred, embodiment utilises amino acid substitution and/or deletion and/or insertion and/or addition (which may be effected by recombinant means or by means of peptide synthesis; modifications which involves longer stretches of amino acids can give rise to fusion polypep- tides) .
  • WO 95/05849 discloses a method for down-regulating self-proteins by immunising with analogues of the self-proteins wherein a number of amino acid sequence (s) has been substituted with a corresponding number of amino acid sequence (s) which each comprise a foreign immunodominant T-cell epitope, while at the same time maintaining the overall tertiary structure of the self-protein in the analogue.
  • the modification be it an amino acid insertion, addition, deletion or substitution
  • IL5 e ⁇ -IL5 ex are x B-cell epitope containing subsequences of IL5 which independently are identical or non-identical and which may contain or not contain foreign side groups
  • x is an integer > 3
  • nl-nx are x integers > 0 (at least one is > 1)
  • MOD ⁇ -MOD x are x modifications introduced between the preserved B-cell epitopes
  • S ⁇ s x are x integers > 0 (at least one is > 1 if no side groups are introduced in the IL5 e sequences) .
  • the invention allows for all kinds of permutations of the original IL5 sequence, and all kinds of modifications therein.
  • modified IL5 obtained by omission of parts of the IL5 sequence which e.g. exhibit adverse effects in vivo or omission of parts which could give rise to undesired immunological reactions.
  • Modified versions which react to the same extent with the antiserum as does IL5 must be regarded as having the same overall tertiary structure as IL5 whereas analogues exhibiting a limited (but still significant and specific) reactivity with such an antiserum are regarded as having maintained a substantial fraction of the original B-cell epitopes.
  • a selection of monoclonal antibodies reactive with distinct epitopes on IL5 can be prepared and used as a test panel.
  • This approach has the advantage of allowing 1) an epitope mapping of IL5 and 2) a mapping of the epitopes which are maintained in the analogues prepared.
  • a third approach would be to resolve the 3-dimen- sional structure of IL5 or of a biologically active truncate thereof (cf. above) and compare this to the resolved three-dimensional structure of the analogues prepared.
  • Three-dimensional structure can be resolved by the aid of X-ray diffraction studies and NMR-spectroscopy . Further information relating to the tertiary structure can to some extent be obtained from circular dichroism studies which have the advantage of merely requiring the polypeptide in pure form (whereas X-ray diffraction requires the provision of crystallized polypeptide and NMR requires the provision of isotopic variants of the polypeptide) in order to provide useful information about the tertiary structure of a given molecule.
  • X- ray diffraction and/or NMR are necessary to obtain conclusive data since circular dichroism can only provide indirect evidence of correct 3-dimensional structure via information of secondary structure elements .
  • One preferred embodiment of the invention utilises multiple presentations of B-lymphocyte epitopes of IL5 (i.e. formula I wherein at least one B-cell epitope is present in two positions) .
  • This effect can be achieved in various ways, e.g. by simply preparing fusion polypeptides comprising the structure (IL5) m , where is an integer > 2 and then introduce the modifications discussed herein in at least one of the IL5 sequences, or alternatively, inserted between at least two of the IL5 amino acid sequences. It is preferred that the modifications introduced includes at least one duplication of a B- lymphocyte epitope and/or the introduction of a hapten.
  • the introduction of a foreign T-cell epitope can be accomplished by introduction of at least one amino acid insertion, addition, deletion, or substitution.
  • the normal situation will be the introduction of more than one change in the amino acid sequence (e.g. insertion of or substitution by a complete T-cell epitope) but the important goal to reach is that the IL5 analogue, when processed by an antigen presenting cell (APC) , will give rise to such a foreign immunodominant T-cell epitope being presented in context of an MCH Class II molecule on the surface of the APC.
  • APC antigen presenting cell
  • the introduction of a foreign T ⁇ epitope can be accomplished by providing the remaining amino acids of the foreign epitope by means of amino acid insertion, addition, deletion and substitution. In other words, it is not necessary to introduce a complete T H epitope by insertion or substitution.
  • the number of amino acid insertions, de- letions, substitutions or additions is at least 2, such as 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, and 25 insertions, substitutions, additions or deletions. It is furthermore preferred that the number of amino acid insertions, substitutions, additions or deletions is not in excess of 150, such as at most 100, at most 90, at most 80, and at most 70. It is especially preferred that the number of substitutions, insertions, deletions, or additions does not exceed 60, and in particular the number should not exceed 50 or even 40. Most preferred is a number of not more than 30.
  • Preferred embodiments of the invention includes modification by introducing at least one foreign immunodominant T H epitope. It will be understood that the question of immune dominance of a T H epitope depends on the animal species in question.
  • the term “immunodominance” simply refers to epitopes which in the vaccinated individual gives rise to a significant immune response, but it is a well-known fact that a T H epitope which is immunodominant in one individual is not necessarily immunodominant in another individual of the same species, even though it may be capable of binding MHC-II molecules in the latter individual.
  • T H epitopes Another important point is the issue of MHC restriction of T H epitopes.
  • naturally occurring T H epitopes are MHC restricted, i.e. a certain peptide constituting a T H epitope will only bind effectively to a subset of MHC Class II molecules. This in turn has the effect that in most cases the use of one specific T H epitope will result in a vaccine component which is effective in a fraction of the population only, and depending on the size of that fraction, it can be necessary to include more T H epitopes in the same molecule, or alternatively prepare a multi-component vaccine wherein the components are IL5 variants which are distinguished from each other by the nature of the T H epitope introduced.
  • a vaccine composition contain- ing 3 foreign T-cell epitopes having response frequencies in the population of 0.8, 0.7, and 0.6, respectively, would give
  • ⁇ j is the sum of frequencies in the population of allelic haplotypes encoding MHC molecules which bind any one of the T-cell epitopes in the vaccine and which belong to the j th of the 3 known HLA loci (DP, DR and DQ) ; in practice, it is first determined which MHC molecules will recognize each T- cell epitope in the vaccine and thereafter these MHC molecules are listed by type (DP, DR and DQ) - then, the individual frequencies of the different listed allelic haplotypes are summed for each type, thereby yielding ⁇ , ⁇ 2 , and fo .
  • v 3 is the sum of frequencies in the population of allelic haplotypes encoding MHC molecules which bind the i th T- cell epitope in the vaccine and which belong to the j th of the 3 known HLA loci (DP, DR and DQ) .
  • DP i th T- cell epitope
  • DQ 3 known HLA loci
  • T-cell epitopes to be introduced in the IL5 analogue, it is important to include all knowledge of the epitopes which is available: 1) The frequency of respon- ders in the population to each epitope, 2) MHC restriction data, and 3) frequency in the population of the relevant haplotypes .
  • T- cell epitopes which are active in a large proportion of individuals of an animal species or an animal population and these are preferably introduced in the vaccine, thereby reducing the need for a very large number of different IL5 analogues in the same vaccine.
  • the promiscuous epitope can according to the invention be a naturally occurring human T-cell epitope such as epitopes from tetanus toxoid (e.g. the P2 and P30 epitopes), diphtheria toxoid, Influenza virus hemagluttinin (HA) , and P. falciparum CS antigen.
  • tetanus toxoid e.g. the P2 and P30 epitopes
  • diphtheria toxoid e.g. the P2 and P30 epitopes
  • Influenza virus hemagluttinin (HA) Influenza virus hemagluttinin
  • P. falciparum CS antigen a naturally occurring human T-cell epitope
  • the epitope can be any artificial T-cell epitope which is capable of binding a large proportion of MHC Class II molecules.
  • the pan DR epitope peptides PADRE
  • the most effective PADRE peptides disclosed in these papers carry D- a ino acids in the C- and N-termini in order to improve stability when administered.
  • the present invention primarily aims at incorporating the relevant epitopes as part of the modified IL5 which should then subsequently be broken down enzymatically inside the lysosomal compartment of APCs to allow subsequent presentation in the context of an MHC-II molecule and therefore it is not expedient to incorporate D- a ino acids in the epitopes used in the present invention.
  • PADRE peptide is the one having the amino acid sequence AKFVAAWTLKAAA (SEQ ID NO: 65) or an immunologically effective subsequence thereof.
  • AKFVAAWTLKAAA SEQ ID NO: 65
  • T-cell epitopes which should be present in the IL5 analogues used in the inventive method.
  • Such super-promiscuous epitopes will allow for the most simple embodiments of the invention wherein only one single modified IL5 is presented to the vac- cinated animal's immune system.
  • the modification of IL5 can also include the introduction of a first moiety which targets the modified IL5 to an APC or a B-lymphocyte.
  • the first mo- iety can be a specific binding partner for a B-lymphocyte specific surface antigen or for an APC specific surface antigen.
  • the moiety can be a carbohydrate for which there is a receptor on the B-lymphocyte or on the APC (e.g. mannan or mannose) .
  • the second moiety can be a hapten.
  • an antibody fragment which specifically recognizes a surface molecule on APCs or lymphocytes can be used as a first moiety (the surface molecule can e.g. be an FC ⁇ receptor of macrophages and monocytes, such as FC ⁇ RI or, alternatively any other specific surface marker such as CD40 or CTLA-4) . It should be noted that all these exemplary targeting molecules can be used as part of an adjuvant also, cf . below.
  • modified IL5 polypeptide As an alternative or supplement to targeting the modified IL5 polypeptide to a certain cell type in order to achieve an enhanced immune response, it is possible to increase the level of responsiveness of the immune system by including the above- mentioned second moiety which stimulates the immune system.
  • second moieties are cytokines, and heat-shock proteins or molecular chaperones, as well as effective parts thereof.
  • Suitable cytokines to be used according to the invention are those which will normally also function as adjuvants in a vac- cine composition, i.e. for instance interferon ⁇ (IFN- ⁇ ),
  • IFN- ⁇ interferon ⁇
  • cytokine molecule may suffice as the second moiety.
  • IL-1 interleukin 1
  • IL-2 interleukin 2
  • IL-4 interleukin 4
  • IL-6 interleukin 6
  • IL-12 interleukin 12
  • IL-13 interleukin 13
  • GM-CSF granulocyte- macrophage colony stimulating factor
  • suitable heat-shock proteins or molecular chaperones used as the second moiety can be HSP70, HSP90, HSC70, GRP94 (also known as gp96, cf. Wearsch PA et al . 1998, Biochemistry 37: 5709-19), and CRT (calreticulin) .
  • the second moiety can be a toxin, such as li- steriolycin (LLO) , lipid A and heat-labile enterotoxin.
  • LLO li- steriolycin
  • lipid A lipid A
  • heat-labile enterotoxin a number of mycobacterial derivatives such as MDP (muramyl dipeptide) and the trehalose diesters TDM and TDE are interesting possibilities.
  • the possibility of introducing a third moiety which enhances the presentation of the modified IL5 to the immune system is an important embodiment of the invention.
  • the art has shown several examples of this principle. For instance, it is known that the palmitoyl lipidation anchor in the Borrelia burgdorferi protein OspA can be utilised so as to provide self-adjuvating polypeptides (cf. e.g. WO 96/40718). It seems that the lipidated proteins form up micelle-like structures with a core consisting of the lipidation anchor parts of the polypeptides and the remaining parts of the molecule protru- ding therefrom, resulting in multiple presentations of the antigenic determinants.
  • lipidation anchors e.g. a myristyl group, a myristyl group, a farnesyl group, a geranyl-geranyl group, a GPI-anchor, and an N-acyl diglyceride group
  • lipidation anchors e.g. a myristyl group, a myristyl group, a farnesyl group, a geranyl-geranyl group, a GPI-anchor, and an N-acyl diglyceride group
  • C3d fragment of complement factor C3 or C3 itself cf. Dempsey et al . , 1996, Science 271, 348-350 and Lou & Kohler, 1998, Nature Biotechnology 16, 458-462 .
  • An alternative embodiment of the invention which also results in the preferred presentation of multiple (e.g. at least 2) copies of the important epitopic regions of IL5 to the immune system is the covalent or non-covalent coupling of IL5, subse- quence or variants thereof to certain carrier molecules.
  • polymers can be used, e.g. carbohydrates such as dextran, cf. e.g. Lees A et al . , 1994, Vaccine 12: 1160-1166; Lees A et ai . , 1990, J Immunol. 145: 3594-3600, but also man- nose and mannan are useful alternatives.
  • Integral membrane proteins from e.g. E. coli and other bacteria are also useful conjugation partners.
  • the traditional carrier molecules such as keyhole limpet hemocyanin (KLH) , tetanus toxoid, diphtheria toxoid, and bovine serum albumin (BSA) are also preferred and useful conjugation partners.
  • IL5 Certain areas of native IL5 are believed to be superiorly suited for performing modifications. It is predicted that modifications in at least one of loops 1-3 or in the amino acid residues C-terminal to helix D (said loops and said helix D corresponding to those shown in Fig. 3 for human and murine IL5) will be most likely to produce the desired constructs and vaccination results. Considerations underlying these chosen areas are a) preservation of known and predicted B-cell epitopes, b) preservation of tertiary and quaternary structures etc, cf. also the discussion in the preamble to the examples. At any rate, as discussed above, it is fairly easy to screen a set of modified IL5 molecules which have all been subjected to introduction of a T-cell epitope in different locations.
  • the IL5 polypeptide discussed above is a human IL5 polypeptide.
  • the human IL5 polypeptide has been modified by substituting at least one amino acid sequence in SEQ ID NO: 1 with at least one amino acid sequence of equal or different length and containing a foreign T H epitope, wherein substituted amino acid residues are selected from the group consisting of residues 87-90, residues 32-43, residues 59-64, residues 86-91, and residues 110-113.
  • substituted amino acid residues are selected from the group consisting of residues 87-90, residues 32-43, residues 59-64, residues 86-91, and residues 110-113.
  • the formulation of the polypeptide follows the principles generally acknowledged in the art.
  • vaccines which contain peptide sequences as active ingredients are generally well understood in the art, as exemplified by U.S. Patents 4,608,251; 4,601,903; 4,599,231; 4,599,230; 4,596,792; and 4,578,770, all incorporated herein by reference.
  • such vaccines are prepared as in- jectables either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid prior to injection may also be prepared.
  • the preparation may also be emulsified.
  • the active immunogenic ingredient is often mixed with excipients which are pharmaceutically acceptable and compatible with the active ingredient.
  • Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol, or the like, and combinations thereof.
  • the vaccine may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents, or adjuvants which enhance the effectiveness of the vaccines; cf. the detailed discussion of adjuvants below.
  • the vaccines are conventionally administered parenterally, by injection, for example, either subcutaneously, intracutane- ously, intradermally, subdermally or intramuscularly.
  • Addi- tional formulations which are suitable for other modes of administration include suppositories and, in some cases, oral, buccal, sublinqual, intraperitoneal, intravaginal, anal, epi- dural, spinal, and intracranial formulations.
  • traditional binders and carriers may include, for example, polyalkalene glycols or triglycerides; such suppositories may be formed from mixtures containing the active ingredient in the range of 0.5% to 10%, preferably 1-2%.
  • Oral formulations include such normally employed excipients as, for exam- pie, pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, and the like. These compositions take the form of solutions, suspensions, tablets, pills, capsules, sustained release formulations or powders and contain 10-95% of active in- gredient, preferably 25-70%.
  • cholera toxin is an interesting formulation partner (and also a possible conjugation partner) .
  • the polypeptides may be formulated into the vaccine as neutral or salt forms.
  • Pharmaceutically acceptable salts include acid addition salts (formed with the free amino groups of the peptide) and which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic a- cids as acetic, oxalic, tartaric, mandelic, and the like. Salts formed with the free carboxyl groups may also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylamino ethanol, histidine, procaine, and the like.
  • the vaccines are administered in a manner compatible with the dosage formulation, and in such amount as will be therapeutically effective and immunogenic.
  • the quantity to be administered depends on the subject to be treated, including, e.g., the capacity of the individual's immune system to mount an immune response, and the degree of protection desired.
  • Suitable dosage ranges are of the order of several hundred micrograms active ingredient per vaccination with a preferred range from about 0.1 ⁇ g to 2,000 ⁇ g (even though higher amounts in the 1- 10 mg range are contemplated) , such as in the range from about 0.5 ⁇ g to 1,000 ⁇ g, preferably in the range from 1 ⁇ g to 500 ⁇ g and especially in the range from about 10 ⁇ g to 100 ⁇ g .
  • Suitable regimens for initial administration and booster shots are also variable but are typified by an initial administration followed by subsequent inoculations or other administrations .
  • the manner of application may be varied widely. Any of the conventional methods for administration of a vaccine are applicable. These include oral application on a solid physiologically acceptable base or in a physiologically acceptable dispersion, parenterally, by injection or the like.
  • the dosage of the vaccine will depend on the route of administration and will vary according to the age of the person to be vaccinated and the formulation of the antigen.
  • polypeptides of the vaccine are sufficiently immu- nogenic in a vaccine, but for some of the others the immune response will be enhanced if the vaccine further comprises an adjuvant substance.
  • an adjuvant which can be demonstrated to facilitate breaking of the autotolerance to autoantigens; in fact, this is essential in cases where unmodified IL5 is used as the active ingredient in the autovac- cine.
  • suitable adjuvants are selected from the group consisting of an immune targeting adjuvant; an immune modulating adjuvant such as a toxin, a cytokine, and a mycobacterial derivative; an oil formulation; a polymer; a micelle forming adjuvant; a saponin; an immunostimulating complex matrix (ISCOM matrix); a particle; DDA; aluminium adjuvants; DNA adjuvants; ⁇ -inulin; and an encapsulating adjuvant.
  • an immune targeting adjuvant an immune modulating adjuvant such as a toxin, a cytokine, and a mycobacterial derivative
  • an oil formulation a polymer
  • a micelle forming adjuvant a saponin
  • an immunostimulating complex matrix ISCOM matrix
  • adjuvants include use of agents such as aluminium hydroxide or phosphate (alum), commonly used as 0.05 to 0.1 percent solution in buffered saline, admixture with synthetic polymers of sugars (e.g. Carbopol®) used as 0.25 percent solution, aggregation of the protein in the vaccine by heat treatment with temperatures ranging between 70° to 101°C for 30 second to 2 minute periods respectively and also aggregation by means of cross-linking agents are possible. Aggregation by reactivation with pepsin treated antibodies (Fab frag- ments) to albumin, mixture with bacterial cells such as C.
  • agents such as aluminium hydroxide or phosphate (alum), commonly used as 0.05 to 0.1 percent solution in buffered saline, admixture with synthetic polymers of sugars (e.g. Carbopol®) used as 0.25 percent solution, aggregation of the protein in the vaccine by heat treatment with temperatures ranging between 70° to 101°C for 30 second to 2 minute periods respectively
  • parvum or endotoxins or lipopolysaccharide components of gram- negative bacteria emulsion in physiologically acceptable oil vehicles such as mannide mono-oleate (Aracel A) or emulsion with 20 percent solution of a perfluorocarbon (Fluosol-DA) used as a block substitute may also be employed. Admixture with oils such as squalene and IFA is also preferred.
  • DDA dimethyldioctadecylammonium bromide
  • DNA and ⁇ -inulin are interesting candidates for an adjuvant as is DNA and ⁇ -inulin, but also Freund's complete and incomplete adjuvants as well as quillaja saponins such as QuilA and QS21 are interesting as is RIBI .
  • Further possibilities are monophos- phoryl lipid A (MPL) , the above mentioned C3 and C3d, and u- ramyl dipeptide (MDP) .
  • MPL monophos- phoryl lipid A
  • C3 and C3d the above mentioned C3 and C3d
  • MDP u- ramyl dipeptide
  • Liposome formulations are also known to confer adjuvant effects, and therefore liposome adjuvants are preferred according to the invention.
  • immunostimulating complex matrix type (ISCOM® matrix) adjuvants are preferred choices according to the invention, especially since it has been shown that this type of adjuvants are capable of up-regulating MHC Class II expression by APCs.
  • An ISCOM® matrix consists of (optionally fractionated) saponins (triterpenoids) from Quillaja saponaria, cholesterol, and phospholipid.
  • the resulting particulate formulation When admixed with the immunogenic protein, the resulting particulate formulation is what is known as an ISCOM particle where the saponin constitutes 60-70% w/w, the cholesterol and phospholipid 10-15% w/w, and the protein 10-15% w/w.
  • the saponin constitutes 60-70% w/w
  • the cholesterol and phospholipid 10-15% w/w constitutes 60-70% w/w
  • the protein 10-15% w/w the protein 10-15% w/w.
  • Details relating to composition and use of immunostimulating complexes can e.g. be found in the above-mentioned text-books dealing with adjuvants, but also Morein B et al . , 1995, Clin. Immunother. 3: 461-475 as well as Barr IG and Mitchell GF, 1996, Immunol, and Cell Biol. 74: 8-25 (both incorporated by reference herein) provide useful instructions for the preparation of complete immunostimulating complexes.
  • Another highly interesting (and thus, preferred) possibility of achieving adjuvant effect is to employ the technique described in Gosselin et al . , 1992 (which is hereby incorporated by reference herein) .
  • the presentation of a relevant antigen such as an antigen of the present invention can be en- hanced by conjugating the antigen to antibodies (or antigen binding antibody fragments) against the Fc ⁇ receptors on mono- cytes/macrophages .
  • Especially conjugates between antigen and anti-Fc ⁇ RI have been demonstrated to enhance immunogenicity for the purposes of vaccination.
  • cytokines targeting and immune modulating substances (i . a . cytokines) mentioned above as candidates for the first and second moieties in the modified versions of IL5.
  • synthetic inducers of cytokines like poly I:C are possibilities.
  • Suitable mycobacterial derivatives are selected from the group consisting of muramyl dipeptide, complete Freund's adjuvant, RIBI, and a diester of trehalose such as TDM and TDE .
  • Suitable immune targeting adjuvants are selected from the group consisting of CD40 ligand and CD40 antibodies or specifically binding fragments thereof (cf . the discussion above), mannose, a Fab fragment, and CTLA-4.
  • Suitable polymer adjuvants are selected from the group consisting of a carbohydrate such as dextran, PEG, starch, man- nan, and mannose; a plastic polymer such as; and latex such as latex beads.
  • VLN virtual lymph node
  • the VLN (a thin tubular device) mimics the structure and function of a lymph node. Insertion of a VLN under the skin creates a site of sterile inflammation with an upsurge of cytokines and chemokines. T- and B-cells as well as APCs rapidly respond to the danger signals, home to the in- flamed site and accumulate inside the porous matrix of the VLN.
  • the vaccine should be administered at least once a year, such as at least 1, 2, 3, 4, 5, 6, and 12 times a year. More specifically, 1-12 times per year is expected, such as 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 times a year to an individual in need thereof. It has previously been shown that the memory immunity induced by the use of the preferred autovaccines according to the invention is not permanent, and therefor the immune system needs to be periodically challenged with the analogues.
  • the vaccine according to the invention may comprise several different polypeptides in order to increase the immune response, cf. also the discussion above concerning the choice of foreign T-cell epitope introductions.
  • the vaccine may comprise two or more polypeptides, where all of the polypeptides are as defined above.
  • the vaccine may consequently comprise 3-20 different modified or unmodified polypeptides, such as 3-10 different polypeptides. However, normally the number of polypeptides will be sought kept to a minimum such as 1 or 2 polypeptides.
  • nucleic acid immunisation As an alternative to classic administration of a peptide-based vaccine, the technology of nucleic acid vaccination (also known as “nucleic acid immunisation”, “genetic immunisation”, and “gene immunisation”) offers a number of attractive features .
  • nucleic acid vaccination does not require resource consuming large-scale production of the immunogenic agent (e.g. in the form of industrial scale fermentation of microorganisms producing modified IL5) . Furthermore, there is no need to device purification and refolding schemes for the immunogen.
  • nucleic acid vaccination relies on the biochemical apparatus of the vaccinated individual in order to produce the expression product of the nucleic acid introduced, the optimum posttranslational processing of the expression product is expected to occur; this is especially important in the case of autovaccination, since, as mentioned above, a significant fraction of the original IL5 B-cell epitopes should be preserved in the modified molecule, and since B-cell epitopes in principle can be constituted by parts of any (bio)molecule (e.g. carbohydrate, lipid, protein etc.). Therefore, native glycosylation and lipidation patterns of the immunogen may very well be of importance for the overall immunogenicity and this is expected to be ensured by having the host producing the immunogen.
  • bio bio
  • a preferred embodiment of the invention comprises effecting presentation of modified IL5 to the immune system by introducing nucleic acid(s) encoding the modified IL5 into the animal's cells and thereby obtaining in vi vo expression by the cells of the nucleic acid(s) introduced.
  • the introduced nucleic acid is preferably DNA which can be in the form of naked DNA, DNA formulated with charged or uncharged lipids, DNA formulated in liposomes, DNA included in a viral vector, DNA formulated with a transfec- tion-facilitating protein or polypeptide, DNA formulated with a targeting protein or polypeptide, DNA formulated with Calcium precipitating agents, DNA coupled to an inert carrier molecule, DNA encapsulated in a polymer, e.g. in PLGA (cf . the microencapsulation technology described in WO 98/31398) or in chitin or chitosan, and DNA formulated with an adjuvant.
  • DNA which can be in the form of naked DNA, DNA formulated with charged or uncharged lipids, DNA formulated in liposomes, DNA included in a viral vector, DNA formulated with a transfec- tion-facilitating protein or polypeptide, DNA formulated with a targeting protein or polypeptide, DNA formulated with Calcium precipitating agents, DNA
  • nucleic acid vaccines can suitably be administered intra- veneously and intraarterially .
  • nucleic acid vaccines can be administered by use of a so-called gene gun, and hence also this and equivalent modes of administration are regarded as part of the present invention.
  • VLN the use of a VLN in the administration of nucleic acids has been reported to yield good results, and therefore this particular mode of administration is particularly preferred.
  • the nucleic acid(s) used as an immunization agent can contain regions encoding the 1 st , 2 nd and/or 3 rd moieties, e.g. in the form of the immunomodulating substances described above such as the cytokines discussed as useful adjuvants.
  • a preferred version of this embodiment encompasses having the coding region for the analogue and the coding region for the immunomodulator in different reading frames or at least under the control of different promoters. Thereby it is avoided that the analogue or epitope is produced as a fusion partner to the immunomodulator.
  • two distinct nucleotide fragments can be used, but this is less preferred because of the advantage of ensured co-expression when having both coding regions included in the same molecule.
  • the invention also relates to a composition for inducing production of antibodies against IL5, the composition comprising a nucleic acid fragment or a vector of the invention (cf. the discussion of vectors below) , and a pharmaceutically and immunologically acceptable vehicle and/or carrier and/or adjuvant as discussed above.
  • the IL5 variant-encoding nucleic acid is introduced in the form of a vector wherein expression is under control of a viral promoter.
  • vectors and DNA fragments according to the inven- tion, cf. the discussion below.
  • detailed disclosures relating to the formulation and use of nucleic acid vaccines are available, cf. Donnelly JJ et al , 1997, Annu. Rev. Immunol. 15: 617-648 and Donnelly JJ et al . , 1997, Life Sciences 60: 163-172. Both of these references are incorporated by refe- rence herein.
  • a third alternative for effecting presentation of modified IL5 to the immune system is the use of live vaccine technology.
  • presentation to the immune system is effected by administering, to the animal, a non-pathogenic microorganism which has been transformed with a nucleic acid fragment encoding a modified IL5 or with a vector incorpora- ting such a nucleic acid fragment.
  • the non-pathogenic microorganism can be any suitable attenuated bacterial strain (attenuated by means of passaging or by means of removal of pathogenic expression products by recombinant DNA technology) , e.g. Mycobacteri um bovis BCG., non-pathogenic Streptococcus spp., E. coli , Salmonella spp .
  • the nucleic acid fragment of the invention discussed below can be incorporated in a non-virulent viral vaccine vector such as a vaccinia strain or any other suitable pox virus.
  • a non-virulent viral vaccine vector such as a vaccinia strain or any other suitable pox virus.
  • the non-pathogenic microorganism or virus is administered only once to the animal, but in certain cases it may be necessary to administer the microorganism more than once in a lifetime in order to maintain protective immunity. It is even contemplated that immunization schemes as those detailed above for polypeptide vaccination will be useful when using live or virus vaccines.
  • live or virus vaccination is combined with pre- vious or subsequent polypeptide and/or nucleic acid vaccination.
  • pre- vious or subsequent polypeptide and/or nucleic acid vaccination it is possible to effect primary immunization with a live or virus vaccine followed by subsequent booster immunizations using the polypeptide or nucleic acid approach.
  • the microorganism or virus can be transformed with nucleic acid(s) containing regions encoding the 1 st , 2 nd and/or 3 rd moieties, e.g. in the form of the immunomodulating substances described above such as the cytokines discussed as useful ad- juvants.
  • a preferred version of this embodiment encompasses having the coding region for the analogue and the coding region for the immunomodulator in different reading frames or at least under the control of different promoters. Thereby it is avoided that the analogue or epitopes are produced as fusion partners to the immunomodulator.
  • two distinct nucleotide fragments can be used as transforming agents.
  • having the 1 st and/or 2 nd and/or 3 rd moieties in the same reading frame can provide as an expression product, an analogue of the invention, and such an embodiment is espe- cially preferred according to the present invention.
  • an important embodiment of the method of the invention for down-regulating IL5 activity comprises treating and/or preventing and/or ameliorating asthma or other chronic allergic conditions characterized by eosinophilia, the method comprising down-regulating IL5 activity according to the method of the invention to such an extent that the number of eosinophil cells is significantly reduced.
  • such a significant reduction in eosinophil cell numbers is at least 20% compared to the eosinophil number prior to treatment, but higher percentages are contemplated, such as at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80% and even at least 90%.
  • the reduction may be systemic or, more often, locally in e.g. the lungs .
  • Eosinophil cell numbers are determined by methods known in the art, typically using microscopy of a suitable sample (such as a BAL fluid) and counting the number of eosinophil cells manually under microscope. Alternatively, eosinophil numbers can be counted using flow cytometric methods or any other convenient method of cytometry capable of distinguishing eosinophils.
  • the present invention is based on the concept of immunising individuals against the IL5 antigen in order to indirectly obtain a reduction in eosinophil cell numbers.
  • the preferred way of obtaining such an immunization is to use modified versions of IL5, thereby providing molecules which have not previously been disclosed in the art.
  • modified IL5 molecules discussed herein are inventive in their own right, and therefore an important part of the invention pertains to an IL5 analogue which is derived from an animal IL5 wherein is introduced a modification which has as a result that immunization of the animal with the analogue induces production of antibodies cross-reacting with the unmodified IL5 polypeptide.
  • the nature of the modification conforms with the types of modifications described above when discussing various embodiments of the method of the invention when using modified IL5.
  • any disclosure presented herein pertaining to modified IL5 molecules are relevant for the purpose of de- scribing the IL5 analogues of the invention, and any such disclosures apply mutati s mutandi s to the description of these analogues .
  • modified IL5 molecules com- prise modifications which results in a polypeptide having a sequence identity of at least 70% with IL5 or with a subsequence thereof of at least 10 amino acids in length. Higher sequence identities are preferred, e.g. at least 75% or even at least 80% or 85%.
  • the sequence identity for proteins and nucleic acids can be calculated as (N re f - N di f) - 100/N ref , wherein N dif is the total number of non-identical residues in the two sequences when aligned and wherein N ref is the number of residues in one of the sequences.
  • the invention also pertains to compositions useful in exercising the method of the invention.
  • the invention also relates to an immunogenic composition comprising an immuno- genically effective amount of an IL5 polypeptide which is a self-protein in an animal, said IL5 polypeptide being formulated together with an immunologically acceptable adjuvant so as to break the animal's autotolerance towards the IL5 polypeptide, the composition further comprising a pharmaceutically and immunologically acceptable vehicle and/or carrier.
  • this part of the invention pertains to the formulations of naturally occurring IL5 polypeptides which have been described in connection with embodiments of the method of the invention.
  • the invention also relates to an immunogenic composition com- prising an immunologically effective amount of an IL5 analogue defined above, said composition further comprising a pharmaceutically and immunologically acceptable diluent and/or vehicle and/or carrier and/or excipient and optionally an adjuvant.
  • this part of the invention concerns for- mulations of modified IL5, essentially as described herein- above.
  • the choice of adjuvants, carriers, and vehicles is accordingly in line with what has been discussed above when referring to formulation of modified and unmodified IL5 for use in the inventive method for the down-regulation of IL5.
  • polypeptides are prepared according to methods well-known in the art. Longer polypeptides are normally prepared by means of recombinant gene technology including introduction of a nucleic acid sequence encoding the IL5 analogue into a suitable vector, transformation of a suitable host cell with the vector, expression of the nucleic acid sequence, recovery of the expression product from the host cells or their culture supernatant, and subsequent purification and optional further modification, e.g. refolding or derivatization.
  • Shorter peptides are preferably prepared by means of the well- known techniques of solid- or liquid-phase peptide synthesis. However, recent advances in this technology has rendered possible the production of full-length polypeptides and proteins by these means, and therefore it is also within the scope of the present invention to prepare the long constructs by synthetic means.
  • modified IL5 polypeptides can be prepared by means of recombinant gene technology but also by means of chemical synthesis or semisyn- thesis; the latter two options are especially relevant when the modification consists in coupling to protein carriers (such as KLH, diphtheria toxoid, tetanus toxoid, and BSA) and non-proteinaceous molecules such as carbohydrate polymers and of course also when the modification comprises addition of side chains or side groups to an IL5 polypeptide-derived peptide chain.
  • protein carriers such as KLH, diphtheria toxoid, tetanus toxoid, and BSA
  • non-proteinaceous molecules such as carbohydrate polymers
  • nucleic acid fragments encoding modified IL5 are important chemical products.
  • an important part of the invention pertains to a nucleic acid fragment which encodes an IL5 analogue, i.e. an IL5 derived polypeptide which either comprises the natural IL5 sequence to which has been added or inserted a fusion partner or, preferably an IL5 derived polypeptide wherein has been introduced a foreign T-cell epitope by means of insertion and/or addition, preferably by means of substitution and/or deletion.
  • the nucleic acid fragments of the invention are ei- ther DNA or RNA fragments.
  • the nucleic acid fragments of the invention will normally be inserted in suitable vectors to form cloning or expression vectors carrying the nucleic acid fragments of the invention; such novel vectors are also part of the invention. Details concerning the construction of these vectors of the invention will be discussed in context of transformed cells and microorganisms below.
  • the vectors can, depending on purpose and type of application, be in the form of plasmids, phages, cosmids, mini-chromosomes, or virus, but also naked DNA which is only expressed transiently in certain cells is an important vector.
  • Preferred cloning and expression vectors of the invention are capable of autonomous replication, thereby enabling high copy- numbers for the purposes of high-level expression or high- level replication for subsequent cloning.
  • the general outline of a vector of the invention comprises the following features in the 5'-»3' direction and in operable linkage: a promoter for driving expression of the nucleic acid fragment of the invention, optionally a nucleic acid sequence encoding a leader peptide enabling secretion (to the extracellular phase or, where applicable, into the periplasma) of or integration into the membrane of the polypeptide fragment, the nucleic acid fragment of the invention, and optionally a nucleic acid sequence encoding a terminator.
  • a promoter for driving expression of the nucleic acid fragment of the invention optionally a nucleic acid sequence encoding a leader peptide enabling secretion (to the extracellular phase or, where applicable, into the periplasma) of or integration into the membrane of the polypeptide fragment, the nucleic acid fragment of the invention, and optionally a nucleic acid sequence encoding a terminator.
  • the vector when working with vectors to be used for effecting in vivo expression in an animal (i.e. when using the vector in DNA vaccination) it is for security reasons preferred that the vector is not incapa- ble of being integrated in the host cell genome; typically, naked DNA or non-integrating viral vectors are used, the choices of which are well-known to the person skilled in the art.
  • the vectors of the invention are used to transform host cells to produce the modified IL5 polypeptide of the invention.
  • Such transformed cells which are also part of the invention, can be cultured cells or cell lines used for propagation of the nucleic acid fragments and vectors of the invention, or used for recombinant production of the modified IL5 polypeptides of the invention.
  • the transformed cells can be suitable live vaccine strains wherein the nucleic acid fragment (one single or multiple copies) have been inserted so as to effect secretion or integration into the bacterial membrane or cell-wall of the modified IL5.
  • Preferred transformed cells of the invention are microorganisms such as bacteria (such as the species Escherichia [e.g. E. coli ] , Bacill us [e.g. Bacill us subtilis] , Salmonella, or Mycobacteri um [preferably non-pathogenic, e.g. M. bovis BCG] ) , yeasts (such as Saccharomyces cerevi siae) , and protozoans.
  • the transformed cells are derived from a multi- cellular organism such as a fungus, an insect cell, a plant cell, or a mammalian cell. Most preferred are cells derived from a human being, cf . the discussion of cell lines and vectors below.
  • the transformed cell is capable of replicating the nucleic acid fragment of the invention.
  • Cells expressing the nucleic fragment are preferred useful embodiments of the invention; they can be used for small-scale or large-scale preparation of the modified IL5 or, in the case of non-pathogenic bacteria, as vaccine constituents in a live vaccine.
  • the modified IL5 of the invention When producing the modified IL5 of the invention by means of transformed cells, it is convenient, although far from essen- tial, that the expression product is either exported out into the culture medium or carried on the surface of the transformed cell.
  • this stable cell line which carries the vector of the invention and which expresses the nucleic acid fragment encoding the modified IL5.
  • this stable cell line secretes or carries the IL5 analogue of the invention, thereby facilitating purification thereof.
  • plasmid vectors containing replicon and control sequences which are derived from species compatible with the host cell are used in connection with the hosts.
  • the vector ordinarily carries a replication site, as well as marking sequences which are capable of providing phenotypic selection in transformed cells.
  • E. coli is typically transformed using pBR322, a plasmid derived from an E. coli species (see, e.g., Bolivar et al . , 1977).
  • the pBR322 plasmid contains genes for a picillin and tetracycline resistance and thus provides easy means for identifying transformed cells.
  • the pBR plasmid, or other microbial plasmid or phage must also con- tain, or be modified to contain, promoters which can be used by the prokaryotic microorganism for expression.
  • promoters most commonly used in prokaryotic recombinant DNA construction include the B-lactamase (penicillinase) and lactose promoter systems (Chang et al., 1978; Itakura et al . , 1977; Goeddel et al . , 1979) and a tryptophan (trp) promoter system (Goeddel et al . , 1979; EP-A-0 036 776).
  • eukaryotic microbes such as yeast cultures may also be used, and here the promoter should be capable of driving expression.
  • Saccharomyces cerevisiase, or common baker's yeast is the most commonly used among eukaryotic microorganisms, although a number of other strains are commonly available.
  • the plasmid YRp7 for example, is commonly used (Stinchcomb et al., 1979; Kings an et al . , 1979; Tschemper et al . , 1980).
  • This plasmid already contains the trpl gene which provides a selection marker for a mutant strain of yeast lacking the ability to grow in tryptophan for example ATCC No. 44076 or PEP4-1 (Jones, 1977) .
  • the presence of the trpl lesion as a characteristic of the yeast host cell genome then provides an effective environment for detecting transformation by growth in the absence of tryptophan.
  • Suitable promoting sequences in yeast vectors include the promoters for 3-phosphoglycerate kinase (Hitzman et al . , 1980) or other glycolytic enzymes (Hess et al . , 1968; Holland et al .
  • enolase such as enolase, glyceraldehyde-3-phosphate dehydro- genase, hexokinase, pyruvate decarboxylase, phosphofructo- kinase, glucose-6-phosphate iso erase, 3-phosphoglycerate mu- tase, pyruvate kinase, triosephosphate isomerase, phosphoglu- cose isomerase, and glucokinase.
  • the termination sequences associated with these genes are also ligated into the expression vector 3' of the sequence desired to be expressed to provide polyadenylation of the mRNA and termination.
  • promoters which have the additional advantage of tran- scription controlled by growth conditions are the promoter region for alcohol dehydrogenase 2, isocytochrome C, acid phosphatase, degradative enzymes associated with nitrogen metabolism, and the aforementioned glyceraldehyde-3-phosphate dehydrogenase, and enzymes responsible for maltose and galactose utilization.
  • Any plasmid vector containing a yeast-compatible promoter, origin of replication and termination sequences is suitable .
  • cultures of cells derived from multicellular organisms may also be used as hosts.
  • any such cell culture is workable, whether from vertebrate or invertebrate culture.
  • interest has been greatest in vertebrate cells, and propagation of vertebrate in culture (tissue culture) has become a routine procedure in re- cent years (Tissue Culture, 1973) .
  • useful host cell lines are VERO and HeLa cells, Chinese hamster ovary (CHO) cell lines, and W138, BHK, COS-7 293, Spodoptera frugiperda (SF) cells (commercially available as complete expression systems from i . a . Protein Sciences, 1000 Research Parkway, Meriden, CT 06450, U.S.A.
  • Expression vectors for such cells ordinarily include (if necessary) an origin of replication, a promoter located in front of the gene to be expressed, along with any necessary ribosome binding sites, RNA splice sites, polyadenylation site, and transcriptional terminator sequences.
  • control functions on the expression vectors are often provided by viral material.
  • promoters are derived from polyoma, Adenovirus 2, and most frequently Simian Virus 40 (SV40) .
  • the early and late promoters of SV40 virus are particularly useful because both are obtained easily from the virus as a fragment which also contains the SV40 viral origin of replication (Fi- ers et al . , 1978). Smaller or larger SV40 fragments may also be used, provided there is included the approximately 250 bp sequence extending from the Hin i11 site toward the Bgll site located in the viral origin of replication.
  • promoter or control sequences normally associated with the desired gene sequence provided such control sequences are compatible with the host cell systems.
  • An origin of replication may be provided either by construc- tion of the vector to include an exogenous origin, such as may be derived from SV40 or other viral (e.g., Polyoma, Adeno, VSV, BPV) or may be provided by the host cell chromosomal replication mechanism. If the vector is integrated into the host cell chromosome, the latter is often sufficient.
  • an exogenous origin such as may be derived from SV40 or other viral (e.g., Polyoma, Adeno, VSV, BPV) or may be provided by the host cell chromosomal replication mechanism. If the vector is integrated into the host cell chromosome, the latter is often sufficient.
  • IL5 native IL5
  • another part of the invention concerns a method for the identification of a modified IL5 polypeptide which is capable of inducing antibodies against unmodified IL5 in an animal species where the unmodified IL5 polypeptide is a self-protein, the method comprising
  • the "set of mutually distinct modified IL5 polypeptides" is a collection of non-identical modified IL5 polypeptides which have e.g. been selected on the basis of the criteria discussed above (e.g. in combination with studies of circular dichroism, NMR spectra, and/or X-ray diffraction patterns) .
  • the set may consist of only a few members but it is contemplated that the set may contain several hundred members.
  • the set of nucleic acid fragments is a collection of non-identical nucleic acid fragments, each encoding a modified IL5 polypeptide selected in the same manner.
  • the test of members of the set can ultimately be performed in vivo, but a number of in vi tro tests can be applied which narrow down the number of modified molecules which will serve the purpose of the invention.
  • T-cell proliferation can be tested by standardized prolifera- tion assays in vi tro .
  • a sample enriched for T-cells is obtained from a subject and subsequently kept in culture.
  • the cultured T-cells are contacted with APCs of the subject which have previously taken up the modified molecule and processed it to present its T-cell epitopes.
  • the proliferation of T-cells is monitored and compared to a suitable control (e.g. T-cells in culture contacted with APCs which have processed intact, native IL5) .
  • proliferation can be measured by determining the concentration of relevant cytokines released by the T-cells in response to their recognition of foreign T-cells.
  • an immunogenic composition com- prising at least one modified IL5 polypeptide which is capable of inducing antibodies against unmodified IL5 in an animal species where the unmodified IL5 polypeptide is a self-protein, the method comprising admixing the member (s) of the set which significantly induces production of antibodies in the animal species which are reactive with IL5 with a pharmaceutically and immunologically acceptable carrier and/or vehicle and/or diluent and/or excipient, optionally in combination with at least one pharmaceutically and immunologically acceptable adjuvant.
  • an immunogenic composition which as an immunogen contains a nucleic acid fragment encoding a immunogenic IL5 analogue, cf. the discussion of nucleic acid vaccination above.
  • nucleic acid sequences and/or vectors are prepared by methods comprising exercise of a molecular amplification technique such as PCR or by means of nucleic acid synthesis.
  • the exemplary candidates for an IL5 autovaccine are constructed according to the AutoVacTM concept (described in detail in WO 95/05849) by substitution with known promiscuous T cell epitopes into the human IL5 wild type protein.
  • the substitutions are peptide substitutions, where the inserted pep- tide may be of the same or different length than the deleted peptide in the wild-type sequence.
  • the constructs in the murine IL5 se- quence For initial proof of concept by in vivo testing and screening, it was decided to prepare the constructs in the murine IL5 se- quence.
  • the tetanus toxoid epitopes P2 (SEQ ID NO: 23) and P30 (SEQ ID NO: 24) are used as substituting peptides, but any other suitable peptide containing or constituting a promiscuous T H epitope could, according to the present invention, be used.
  • the above considerations of structure conservation and biological activity defines the target areas as any one of loops 1-3 as well as the C-terminal flexible area.
  • Loop 3 is selected as the primary target area since it is structurally separated from the assumed tri-helical folding scaffold. As it is furthermore possible to produce a biologically active monomer, by elongation of loop 3 (Dickason, 1996) , this area holds the possibilities for generating all types of variants: monomer/dimer and active/inactivated.
  • Loop 1 is a second area containing a non-helical stretch of a suitable length for substitutions. Variants from this region would theoretically be active only if capable of dimerising, but since the length of the wild-type loop makes it rather flexible it is reasonable to expect a correct folding of the protein after substitution.
  • Variants containing substitutions in the "loop 2" area will also only be active as di ers .
  • the area that can be substituted is short compared to the inserts and has a central posi- tion in the assumed folding scaffold, two characteristics of loop 2 which might be of hindrance to the correct folding of the protein after substitution.
  • loop 2 is situated opposite to the area interacting with the IL5R, resulting in an expected optimum presentation of the wild-type neutralising epitopes if the modified protein is correctly folded.
  • amino acid sequence of 10 variants initially constructed according to the above considerations are set forth as SEQ ID NOs : 2-11 and 13-22. Further variants constructed at a later stage are set forth in SEQ ID NOs: 27-59 (including both DNA nucleic acid sequences and amino acid sequences) .
  • positions for substitution are indexed according to the murine amino acid residue sequence numbers; the corresponding human positions are given in parentheses .
  • the P2 epitope (SEQ ID NO: 23) is substituted into loop 3 while avoiding elimination of Cys84(86).
  • These variants (SEQ ID NOs: 2 and 28 (human), where amino acids 87-90 or 88-91 are substituted and 13 and 46 (murine) where amino acids 85-88 pr 86-89 are substituted) are potentially active as both monomers (due to the elongation of loop 3) and as dimers.
  • SEQ ID Nos: 28 and 46 are also denoted hIL5.1 and mIL5.1, respectively.
  • the P2 epitope (SEQ ID NO: 23) is substituted into loop 1 while avoiding elimination of Cys42(44).
  • These variants (SEQ ID Nos: 3 and 36 (human) where amino acids 32-43 or 33-43 are substituted and 14 and 56 (murine) where amino acids 30-41 or 31-41 are substituted) are potentially active as dimers only.
  • SEQ ID Nos: 36 and 56 are also denoted hIL5.5 and mIL5.5, respectively.
  • the P2 epitope (SEQ ID NO: 23) is substituted into loop 2.
  • These variants (SEQ ID Nos: 4 and 34 (human) where amino acids 59-64 are substituted and 15 and 50 (murine) where amino acids 57-62 are subsituted) are potentially active as dimers only.
  • SEQ ID Nos: 34 and 50 are also denoted hIL5.4 and mIL5.4, respectively.
  • the P2 epitope (SEQ ID NO: 23) is substituted into loop 3 while eliminating Cys84(86) .
  • These variants (SEQ ID NOs: 5 and 38 (human) where amino acids 86-91 are substituted and 16 and 54 (murine) where amino acids 84-89 are substituted) are in principle similar to the variants of type #1 (SEQ ID NOs: 2 and 28 and 13 and 46) , but the generation of monomer products has been facilitated by inhibiting the formation of disulfide bridging and adjusting the length of loop 3.
  • SEQ ID Nos: 38 and 54 are also denoted hIL5.6 and mIL5.6, respectively.
  • the P2 epitope (SEQ ID NO: 23) is substituted into the amino acids
  • the P30 epitope (SEQ ID NO: 24) is substituted into loop 3 avoiding elimination of Cys84(86).
  • These variants (SEQ ID NOs: 7 and 40 (human) where amino acids 88-91 or 87-90 are substituted and 18 and 58 (murine) where amino acids 85-88 or 86-89 are substituted) are potentially active both as monomers (due to the elongation of loop 3) and as dimers.
  • SEQ ID Nos: 40 and 58 are also denoted hIL5.7 and mIL5.7, respectively.
  • the P30 epitope (SEQ ID NO: 24) is substituted into loop 1, avoiding elimination of Cys42(44).
  • These variants (SEQ ID NOs: 8 and 30 (human) where amino acids 32-43 are substituted and 19 and 48 (murine) where amino acids 30-41 are substituted) are potentially active as dimers only.
  • SEQ ID Nos: 30 and 48 are also denoted hIL5.2 and mIL5.2, respectively.
  • the P30 epitope (SEQ ID NO: 24) is substituted into loop 2.
  • These variants (SEQ ID NOs: 9 and 20 where amino acids 59-64 and 57-62 are substituted, respectively) are potentially active as dimers only.
  • the P30 epitope (SEQ ID NO: 24) is substituted into the C-terminal area succeeding helix D.
  • the P2 epitope (SEQ ID NO: 23) is substituted into loop 3 eliminating Cys84(86) and the P30 epitope (SEQ ID NO: 24) is substituted into the C-terminal area succeeding helix-D.
  • These variants (SEQ ID NOs: 11 and 22) are together with variants of type #12 the only ones containing both epitopes and are poten- tially active monomers.
  • the P2 epitope (SEQ ID NO: 24) is substituted into loop 3 while elimina ting Cys84(86).
  • These variants (SEQ ID NOs: 42 (human) where amino acids 86-91 are substituted and 58 (murine) where amino acids 84-89 are substituted) are in princi- pie similar to the variants of type #6, but the generation of monomer products has been facilitated by inhibiting the formation of disulfide bridging and adjusting the length of loop 3.
  • SEQ ID Nos: 42 and 58 are also denoted hIL5.12 and mIL5.12, respectively.
  • the P2 (SEQ ID NO: 23) and P30 (SEQ ID NO: 24) epitopes are substituted into loop 3 while preserving Cys84(86).
  • These variants (SEQ ID NOs: 44 and 60 where amino acids 88-91 and 86-89 are substituted, respectively) contain both epitopes and are potentially active monomers.
  • SEQ ID NOs: 44 and 60 are also denoted hIL5.13 and mIL5.13, respectively.
  • Recombinant IL5 has been expressed in a number of different expression systems including yeast, insect cells and CHO cells (Tavernier et ai . , 1989).
  • one suitable expression system is E. coli , based on previous studies reporting the use of this host for production hIL5 (Proudfoot et al . , 1990, Graber et a . , 1993).
  • the recombinant protein is expressed as inclusion bodies that are converted into the biologically active dimer upon purification and re-folding (e.g. using the generally applicable refolding methods disclosed in US
  • Dro- sophila melanogaster expression system using S 2 cells (avail- able from Invitrogen) and at present this system is the preferred embodiment for expression of the IL5 analogues of the invention.
  • IL5 variant protein was produced from S2 drosophila cells stably expressing the IL5 constructs. Several different transfection methods were tested, and both Ca 2 P0 4 and Lipofectin were chosen. Two different subclones of S2 cells were used and transfected with Ca 2 P0 4 and Lipofectin, respectively. The two clones were obtained from ATCC and Lars S ⁇ ndergaard of the University of Copenhagen, respectively. Using both methods suitable stable lines were selected expressing mIL5 and mIL5.1 proteins in the 2-10 mg/L range.
  • S2 cells were grown and maintained in Schneider's medium (Sigma) containing 5-10% fetal calf serum (FCS), 0.1% pluronic F68 (Sigma) , penicillin/streptomycin (Life Technologies) grown in shake flasks at 25°C and 120 rpm.
  • FCS fetal calf serum
  • pluronic F68 Sigma
  • penicillin/streptomycin Life Technologies
  • Lipofectin transfections were performed in 250 ml or 1 1 shake flasks. S2 cells were split to 2.5-3 x 10 6 /ml into 50 ml Ex- cell 420 (JRH Biosciences) without antibiotics, and grown overnight in a 250 ml shake flask. The next morning the Lipofectin reagents were prepared: tube 1) 300-1200 ⁇ g plasmid DNA containing the gene of interest, plus 15-60 ⁇ g pCoHYGRO hygromycin selection plasmid (20:1 ratio of plasmids) in 15-45 ml serum and supplement-free medium; tube 2) 1ml Lipofectin in 5 ml serum and supplement-free medium. After 1 hour at room temperature, tubes 1 and 2 were mixed and rested for 15 minutes at room temperature before gently adding to S2 cells. After growing cells overnight new media was added containing full suplements plus 150-300 ⁇ g/ml Hygromycin.
  • Transient and stable lines were induced with either 500 uM copper sulfate or 10 ⁇ M cadmium chloride for 48-72 hours in serum-free Ex-cell 420 medium (JRH Biosciences) .
  • Expression plasmid contained sequence mutations. Hence, S2 cells can be transfected by either calcium phosphate precipitation or Lipofectin. Due to the difference in expression level between plasmids p612 and p767, it seems that the Bip signal peptide is a more efficient leader sequence than the endogenous mIL5 leader in S2 cells.
  • the recombinant protein is purified and characterised.
  • the characterisation of the autovaccine candidates will include analytical chromatography, iso-electric fo- cussing (IEF) , SDS-PAGE, amino acid composition analysis,
  • N-terminal sequence analysis N-terminal sequence analysis, mass spectrometry, low angle laser light scattering, standard spectroscopy, and Circular Dichroism to an extent that precisely document the relevant parameters defining the intended protein product.
  • the His tagged proteins have been purified using a two-step procedure until recently. However, the yield and purity were not as high as expected after the final chelate-step. A new one-step purification procedure has been implied with 3 major advantages achieved: higher yield, higher through-put and higher purity of the final product. Cleavage conditions for removal of the histag have also been established.
  • Expression of the protein is induced by addition of metal ions to the media. These metal-ions have to be removed before application of the protein to the chelate column. Thus, a total of 20 mM EDTA is added to complex the metal-ions and the su- pernatant is then passed over a SP-sepharose column to capture the protein. After washing to remove unbound protein, bound protein is eluted by a step-gradient of NaCl. This step serves two purposes: a concentrating step reducing the volume by a factor of 30, and buffer-exchange.
  • the protein is applied to a Ni 2+ -charged chelate column and unbound protein washed off. Bound protein is then eluted using an Imidazole gradient. All fractions, flow-through and EDTA- washes of the column, are then checked by both SDS-PAGE and dot-blot.
  • the dialyzed material is concentrated until a suitable concentration is achieved (preferably 1 mg/ml) .
  • a suitable concentration preferably 1 mg/ml
  • the received supernatant is centrifuged at 2500 x g tor 15 min (if infection has occurred, it needs centrifugation at 22000 x g for 30 min.
  • the supernatant is then filtered using a 0.45 um filter followed by a 0.22 ⁇ m filter (sometimes it is necessary to filter through a 5 ⁇ m filter first) .
  • buffer A (see step 2) containing 40 mM EDTA, resulting in a final buffer composition of 0.2 M NaH 2 P0 4 , 10% glycerol, 20 mM EDTA, pH 6.0
  • the column is cleaned with 2 CV 1 M NaOH, flow 5 ml/min after each run and re-equilibrated n buffer A.
  • Buffer A 0.2 M NaH 2 P0 4 , 10% glycerol, pH 6.0
  • Buffer B 0.2 M NaH 2 P0 4 , 1 M NaCl, 40 mM Imidazole, 10% glycerol, pH 6.0
  • the supernatant is applied directly to a 70-ml chelate-column charged with ZnCl 2 .
  • bound protein IL5 and contaminants
  • This method takes full advantage of the His tag giving a one-step purification procedure with a high degree of purity of the final product (>95%) .
  • Relevant fractions are pooled and dialyzed twice against 10 X volume of PBS, pH adjusted to 6.9 and concentration of NaCl adjusted to 400 mM.
  • the dialyzed material is concentrated until a suitable concentration is achieved (preferably 1 mg/ml) .
  • a suitable concentration preferably 1 mg/ml
  • a specific protocol follows the following steps 1) The supernatant is filtered through a 0.45 ⁇ m filter to remove impurities and diluted 1:1 with buffer A.
  • a 70-ml Fast Flow chelate column is rinsed with 5 CV water and then charged with 10 CV 10 mM ZnCl 2 , pH 7. After equilibration w th 5 CV A-buffer, the sample is applied using the pump (flow 10 ml/mm) . The flow-through is collected and saved for later analysis. Bound protein is eluted using an Imidazole-gradient going from 0 to 250 mM Imidazole over 30 CV. Finally, the column is stripped by 5 CV of buffer C. Fractions of 10 ml are collected.
  • Buffers A: 20 mM NaH 2 P0 4 , 0.5 M NaCl, 10% glycerol, pH 7.
  • the dialysate is filtered through a 0.22 ⁇ m filter (50 ⁇ l is saved for later analysis) and A 28 o is measured u- sing dialysis-buffer (filtered through 0.45 um) as reference.
  • the volume before and after dialysis is measured and samples showing the dialysis/concentrating step are saved for later analysis by SDS-PAGE (after step 3) .
  • All samples from the dialysis and concentrating step are ana- lyzed by SDS-PAGE and Coomassie-sta ned.
  • the purified protein is stored frozen in aliquots and a sheet describing the sample is filed in the "IL5-protem"-folder .
  • both IL5wt and variant IL5.1 gave the expected N-termmal sequences including the His Tag.
  • a 5-ml HiTrap chelate column (use only dedicated columns) is rinsed with 15 ml water (using a syringe) and then charged with 15 ml 0.1 M N ⁇ S0 4 and washed with 15 ml water.
  • the column is connected to the Akta-system and equilibrated with 2-3 CV A-buffer.
  • the sample is applied using either the loop or pump - depending on the volume (flow 4 ml/min) , the flow-through is collected and saved for later analysis.
  • Bound protein is eluted using an Imi- dazole-gradient going from 0 to 500 mM Imidazole over 20 CV. Fractions of 5 ml are collected. Finally, the column is stripped using 5 CV of buffer B2.
  • Buffer A 0.2 M NaH 2 P0 4 , 0.5 M NaCl, 10 % glycerol, pH 5.0
  • Buffer Bl 0.2 M NaH 2 P0 4 , 0.5 M NaCl, 0.5 M Imidazole, 10 % glycerol, pH 5.0
  • Buffer B2 50 mM Na-acetate, 0.5 M NaCl, 0.1 M EDTA, 10 % gly- cerol, pH 4.5
  • the dialyzed protein is concentrated using either an Amicon apparatus (for volumes larger than 50 ml) or Vivaspm concentrating device (for 10-50 ml). In both cases, the membrane is saturated with 10 ml PBS buffer before the sample is applied. The sample should be concentrated until a concentration of preferably 1 mg/ml is achieved (as measured by A 2S0 ) . The A 2 ⁇ o is measured using the flow-through as reference. The dialyzed, concentrated sample is filtered through a 0.22 ⁇ m filter and marked with an E-nr.
  • the purified and dialyzed/concentrated His tagged IL5 is de-His tagged by the sequential addition of two enzymes, DAP1 and Glutamine cyclotransf erase.
  • DAP1 removes two amino acids from the free N-ter- minus while the QCT
  • the enzyme needs to be activated first:
  • This portion will digest 1 mg of His tagged protein.
  • the His tagged protein is mixed with 150 ⁇ l activated enzyme and incubated at 37°C for 120 min. Samples are withdrawn for SDS-PAGE analysis (10 ⁇ l) after 0, 10, 30, 60 and 120 min. The samples are put on ice to stop the digestion.
  • TAGZyme buffer 20 mM NaP0 4 buffer, pH 7.5; 150 mM NaCl
  • the digested protein (as determined from SDS-PAGE analysis or N-terminal sequencing) is applied to a 1-ml Ni-chelate column equilibrated in PBS. Everything is collected. The flow-through from the appli cation is saved for later analysis .
  • the column is eluted by addition of 3 CV PBS , fractions of 0 . 5 ml are collected . The column is cleaned by washing with 2 CV 0 . 5 M Imidazole , and fractions are saved for analysis .
  • Removal of His tag has been performed small-scale experiments ( 0.1-1 mg) and has not been up-scaled . It should be noted that removal of the tag requires an unblocked and non- modified N-terminus .
  • the His tagged protein is incubated with two enzymes, a dipeptidyl amino peptidase which removes two amino acids at a time and a glutamic acid cyclotransferase which catalyze the conversion of a glutamic acid into a pyro-glutamic acid. This conversion blocks further degradation by the dipeptidyl amino peptidase.
  • the digestion mixture is then passed through a chelate column which should retain the enzymes (which are His tagged) , contaminating proteins binding to the column and non- degraded or partially degraded protein.
  • the de-tagged protein passes the column and is collected in the flow-through. After a second digestion with an enzyme that removes the pyro-glutamic acid, the protein is again passed over a chelate-column to remove the second enzyme. It is expected that the protein needs to be concentrated again at this final stage.
  • the pl of UniHis-IL5wt is 9.5 and the optimum pH-value for the protein seems to be 6. 5-7 . 0 (has not been investigated tho- roughly) .
  • a NaCl-concentration of 400 mM seems to stabilize the protein during concentration.
  • the primary in vi tro screening will be in the form of an enzyme-linked immunosorbent assay (ELISA) :
  • ELISA enzyme-linked immunosorbent assay
  • a conventional ELISA assay can be used to measure titres of auto-antibodies in the serum of vaccinated animals.
  • Antibodies both mono-specific and monoclonal
  • Antibodies towards the human as well as towards the murine IL5 are commercially available from R&D Systems, 614 McKinley Place NE, Minneapolis, MN 55413, USA.
  • the biological activity of the product and/or the neutralising capacity of induced auto-antibodies can be tested in an IL5 bioassay.
  • IL5 bioassays are: Assessment of IL5 induced proliferation of TF1 cells (for human IL5) and assessment of IL5 induced proliferation of BCL1 cells or B13 B cells (for murine IL5) (Callard & Gearing 1994, Dickason et al . , 1994;.
  • the effect on airway responsiveness of the autovaccine can also be tested in an in vi tro assay wherein the trachea from vaccinated mice are removed and placed on a hook in an organ bath. The tension of the trachea after histamine challenge is measured (van Oosterhout et al . , 1995).
  • the cells are plated in complete RPMI medium supplemented with fetal calf serum (FCS) in microtiter plates and incubated with dilution series of murine IL5.
  • FCS fetal calf serum
  • Proliferation of the BCL1 cells is measured by incorporation of tritiated thymidine.
  • Several optimi- zation experiments have been performed using dilution series of purchased recombinant mIL5 (R&D Systems) for stimulation.
  • the variable parameters include: incubation intervals, 3 H- thymidine pulsing intervals, numbers of cells plated per well, fetal calf serum (FCS) concentrations and concentrations of added mIL5.
  • FCS fetal calf serum
  • the BCL1 assay has been used to determine the biological ac- tivity of the following samples expressed from Drosophila S2 cells and purified as described above: HIS-mIL5wt material (E1320), HIS-mIL5wt material (E1422), HIS-mIL5.1 material (E1396) and an "S2-background-preparation” (E0016) .
  • the proliferation in response to one HIS-mIL5wt (E1320) preparation was significantly higher than the proliferation in response to the "S2-background-preparation", whereas the mIL5.1 variant and one wild type preparation (E1422) were determined as biologically inactive.
  • mice Several of the studies investigating the effect of anti-IL5 mAb' s have been successfully performed in mice. Against use of the murine model speaks the fact the IL5 acts as a B-cell growth factor, rendering possible interference with the murine antibody response. However, as shown in a study using IL5 knock-out mice, the T-cell dependent antibody response against ovalbumin as well as cytotoxic T-cell development appeared normal (Kopf et al . , 1996) . As the mouse is also the most practical and economical model in comparison to guinea pigs or monkeys, the ovalbumin sensitised Bal/c mice model of asthma/airway hypersensitivity as used by Hamelman et al. (1997) will be used.
  • Insertion of P2 and P30 epitopes into wildtype mIL5 was done by SOE-PCR with overlapping primers containing the epitope sequences.
  • Wildtype mIL5 gene including leader sequence (SEQ ID NO: 63) was used as template for the PCR reactions .
  • the resulting fragments were digested with Nhel and Notl , purified and cloned into p815 was used as template for the PCR.
  • Wildtype mIL5 was cloned into the pMT Drosophila expression vector series (Invitrogen) by generating a PCR fragment with mIL5 specific primers containing appropriate restriction sites and, in addition, containing sequences encoding a Drosophila Kozak like sequence followed by the Drosophila BiP leader sequence followed by a sequence encoding a U ⁇ I-HIS tag (SEQ ID NO: 25) fused to the 5' end of the sequence encoding mature mIL5. Wildtype mIL5 cDNa sequence was used as template. The resulting fragment was digested with £coRI and Notl and was subsequently cloned into the pMT/V5-HisA vector (Invitrogen) .
  • the resulting plasmid (p818) was used for cloning of epitope containing variants into pMT. These were cloned by digesting the variants made in pcD ⁇ A3.1+ with Sacl and Notl and cloning the resulting fragments into p818. Cloning of variants into pAC5:
  • Wildtype and variants of mIL5 were cloned into the pAC5 constitutive Drosophila expression vector by digestion of variants in pMT with £coRI and Notl and cloning the resulting fragments into the pAC5.
  • l/V5-HisA vector (Invitrogen).
  • IL5 Five lines of plasmids are contemplated containing unmodified IL5 and all or some of the nine IL5 variants.
  • the tag is termed "UNI” or "UNI-His tag” herein) in the pMT/V5/HIS vector for inducible expression in Drosophila, 3) as in 2 but without the His tag, 4) as in 3 but with murine IL5 and 5) human IL5 with the DAPI leader sequence and the 15 aa HIS tag in the vector pVL1393 for expression in the baculo-virus system.
  • Plasmids for DNA- vaccination in the pCI vector Plasmids for DNA- vaccination in the pCI vector :
  • Plasmids for human IL5 expression in Drosophila with the BiP leader sequence, but without the UNI-HIS tag in pMT/V5/HIS Name Ref # Strain # Epitope hIL5m-BiP (pMT/V5-HisA) p908 MR#1256 none hIL5.1m-B ⁇ P (pMT/V5-H ⁇ sA) p909 MR#1257 P2, Loop 3 hIL5.2m-BiP (pMT/V5-HisA) p921 MR#1269 P30, Loop 1 hIL5.3m-B ⁇ P (pMT/V5-H ⁇ sA) p922 MR#1270 P30, Loop 2 hIL5.4m-BiP (pMT/V5-HisA) p923 MR#1271 P2, Loop 2 hIL5.5m-BiP (pMT/V5-HisA) p924 MR#1272 P2, Loop 1 hIL
  • DNA fragments encoding mIL5wt, mIL5.1 and mIL5.5 including the natural leader sequence (SEQ ID NO: 63) were inserted into pcDNA3.1 thus yielding new plasmids p521, 522, and p523.
  • Kozak concensus sequences were inserted upstream of the coding sequences using PCR technology. PCR reactions were performed u- sing p521, p522 and p523 as templates and a forward primer encoding the Kozak sequence immediately upstream of the mIL5 leader start codon.
  • COS cells were trypsinized and plated in DMEM medium supplemented with 10 % FCS in T25 culture flasks. The cells were transfected at day 2 using the Dotap kit (Roche Diagnostics) and harvested at day 5. Culture supernatant, whole cell lysate and membrane enriched preparations were tested in Western blotting to detect anti-mIL5 reactive expression product.
  • the anti-mIL5 reactive product in the cell preparations consistently migrated as 2-3 separate bands of 21-28 kD in SDS-PAGE, whereas the MW of the mIL5 monomer used as standard (expressed in bacculovirus, R&D Systems) is only 15-18 kD.
  • the 21-28 kD substances form dimers so we believe the material is mIL5, possibly in several differently glycosylated forms. DNA vaccination results (see below) clearly support this conclusion.
  • a DNA vaccination study was performed in order to investigate whether antibody responses specific for murine IL5 can be in- prised by immunising mice with naked plasmid DNA encoding 8 different murine IL5 mutants. Since IL5 previously has been reported to play a role in B cell differentiation, it is essential to demonstrate that anti-mIL5 autoantibodies can be generated in mice and B cell tolerance to mIL5 can be broken.
  • mice C3H/Hen mice (H-2 k ) or Balb/cA mice (H-2 d ) , 6-8 weeks old divided into groups of 5 mice each.
  • the mice were anaestesized using hypnorm/dormicum s.c. and injected with expression plasmids encoding ovalbumin (control), mIL5wt (wild type), or the mIL5 variants to be tested.
  • the DNA material was prepared using endofree GigaPrep kits (Qiagen) and dissolved at 1 ⁇ g/ml in 0.15 M NaCl or 0.15 M NaCl containing 0.1% bupivacaine .
  • FIG. 4 A Typical result of a DNA vaccination experiment is shown in Fig. 4.
  • 40 Balb/cA mice were immunized with ovalbumin control plasmid, mIL5wt encoding plasmid or plasmids encoding the mIL5 AutoVac variants mIL5.1 or mIL5.5.
  • 9 out of 9 mice immunized with ovalbumin encoding plasmid developed anti-oval- bumin antibodies, whereas no anti-ovalbumin response was in- prised in mice receiving the mIL5 wild type or mIL5 variant encoding DNA.
  • the main result of the whole series of DNA vaccination experiments is summarized in the table below.
  • the number of respon- ders within an immunisation group differs between the diffe- rent mIL5 AutoVac constructs and is dependent on the mouse strain.
  • the mIL5.2 AutoVac construct is superior to the other variants, being able to induce anti-mIL5 antibody responses in both mouse strains with a penetrance of 100 %.
  • This plasmid (p820) also gave the highest expression levels in the COS transfection assay.
  • ELISA experiments were set up in order to determine whether antibodies specific for the inserted T helper epitope could be detected in anti-mIL5 positive mice.
  • sera from anti-mIL5 positive mice were pooled and tested for reactivity against P2 or P30 peptides which had been immobilised in AquaBind microtiter plates.
  • Antisera induced by DNA vaccination against mIL5.2 in both mouse strains clearly contained reactivity against the inserted P30, whereas none of the other antisera were reactive with P2 or P30. This is probably connected to the higher antibody titers and pene- trance that is generally observed with the mIL5.2 DNA vaccination construct. It should be mentioned that using this ELISA setup we were able to detect anti-P2 reactivity in antisera induced against mIL5.1.
  • the positive anti-mIL5 antiserum pools from the DNA vaccinated mice were also tested in a competive ELISA for their ability to inhibit the interaction between soluble native murine IL5 and monoclonal antibodies TRFK4 or TRFK5, which are both neutralizing antibodies.
  • Dilution series of anti-mIL5 antiserum pools were preincubated with soluble native mIL5 and the sample was added to ELISA plates coated with catching antibody TRFK5.
  • Bound murine IL5 (which was not absorbed by the antisera) was next visualised using layers of biotinylated TRFK4 and subsequently horse radish peroxidase labeled streptavidin.
  • mice 40 DNA vaccinated mice were chosen for testing m an animal model of eosinophilia: 10 Balb/cA mice immunized with mIL5wt DNA, 10 Balb/cA mice immunized with mIL5.2 DNA, 10 C3H/Hen mice immunized with mIL5wt DNA and 10 C3H/Hen mice immunized with mIL5.2 DNA.
  • a sensitization/challengmg regimen with ovalbumin to induce eosinophilia was given to m each of these mice.
  • the mice were sensitized with subcutaneous injections of 50 ⁇ g ovalbumin (OVA) in 0.9 % saline mixed 1:1 with Adjuphos once per week for three weeks.
  • OVA ovalbumin
  • mice Four days after the last OVA sensitization the mice were challenged mtranasally with 12.5 ⁇ g OVA in 0.9 % saline every other day for a total of 3 challenges.
  • Bronchoalveolar lavage fluid (BALF) was collected one day after the last sensitization by cannulatmg the tracheae and washing the airway lumina with 1 ml PBS .
  • BALF cells were spun unto slides at 1,500 rpm for 20 minutes. The slides were dried overnight and stained for 2.5 minutes with May-Grunwald stain (Sigma), washed for 4 minutes in tris buffered saline, stained for 20- 30 minutes with Geimsa stain (1:20 with ddH20; Sigma) and briefly rinsed with ddH20. Stained slides were dried overnight and cell types were identified using light microscopy. Approximately 100-200 cells were counted per slide and 3 slides were counted per mouse. The eosinophil counts were expressed as the number of eosinophils per 100 cells counted.
  • Balb/cA mice are only weakly susceptible to the model. This is supported by anti-ovalbumin ELISA data showing that one week before the BALF collection the anti- ovalbumin titers in serum from the Balb/cA mice were lower than in serum from C3H/Hen.
  • the Balb/cJ substrain is reported to be susceptible to the OVA sensitization/challenge model.
  • mice were immunized with murine IL5 (mIL5) protein and subjected to an ovalbumin intranasal model that induces eosinophils in the lungs of treated mice.
  • mIL5 murine IL5
  • Both the UniHis-mIL5 and the UniHis-mIL5.1 proteins induced antibodies that cross- react with mIL-5 made in sf9 cells from R&D Systems.
  • the eosinophilia model induced high numbers of eosinophils in the OVA control group and the UniHis-mIL5.1 groups, while the numbers of eosinophils were reduced in both the PBS group and the UniHis-mIL5 group. This result led us to believe that the groups may have been mixed.
  • mice 6-8 week old female Balb/c J (M&B) mice were immunized with either 1) nothing, 2) PBS, 3) UniHis-mIL5, or 4) UniHis-mlL- 5.1 in Complete Freund's Ajuvant (CFA; Sigma) and boosted 3 times at three week intervals with antigen in Incomplete Freund's Adjuvant (IFA; Sigma). Sera was collected and tested in an ELISA 10 days after each boost.
  • CFA Complete Freund's Ajuvant
  • IFA Incomplete Freund's Adjuvant
  • Sera were obtained at days 32 (bleed 1) and 54 (bleed 2) after 2 and 3 immunizations, respectively.
  • Polystyrene microtiter plates (Maxisorp, Nunc) were coated with purified HIS-mIL5wt (0.1 ⁇ g/well, E1320) .
  • the reactivities of diluted sera added to the wells were visualised using a goat anti-mouse secondary antibody.
  • OD490 readings of control sera from mice immunized with PBS in Freunds adjuvans were subtracted from the OD490 readings of the test samples.
  • Sera were obtained at day 75 (bleed 3) .
  • Polystyrene microtiter plates (Maxisorp, Nunc) were coated with purchased mIL5 (0.1 ⁇ g/well, R&D cat. no. 405-ML).
  • the reactivities of 1:1000 diluted sera added to the wells were visualised using a goat anti-mouse secondary antibody.
  • the reactivity of TRFK5 (2 ⁇ g/ml) was visualised using a rabbit anti-rat secondary antibody.
  • Anti-P2 ELISA Pools of antisera from HIS-mIL5wt, HIS-mIL5.1 or PBS immunised mice were tested for reactivity against P2 peptide in ELISA. Specialized microtiter plates (Aquabind, M&E Biotech) were coated with 0.5 ⁇ g/well synthetic P2 peptide. The reactivities of diluted sera added to the wells were visualised using a HRP labelled goat anti-mouse secondary antibody (1:2000, Dako) .
  • HIS-tag peptide (UNIZYME) in ELISA.
  • Specialized microtiter plates (AquaBind, M&E Biotech) were coated with 0.5 ⁇ g/well synthetic HIS-tag peptide.
  • HRP labelled goat anti-mouse secondary antibody (1:2000, Dako).
  • Anti-S2 background protein ELISA Anti-S2 background protein ELISA:
  • Eosinophilia Model Balb/c J mice were sensitized with subcutaneous injections of 50 ⁇ g ovalbumin (OVA) in 0.9% saline mixed 1:1 with Adjuphos as alum adjuvant. OVA immunizations were repeated once per week for four weeks. One week after the last OVA sensitization, the mice were challenged with 12.5 ⁇ g OVA in 0.9% saline intranasal every other day for a total of 3 challenges. Bronchoalveolar lavage fluid (BALF) was collected one day after the last sensitization by cannulating the tracheae and washing the airway lumina with 1 ml 0.9% saline, or PBS.
  • BALF Bronchoalveolar lavage fluid
  • BALF cells were spun unto slides at 1,500 rpm for 20 minutes. The slides were dried overnight and stained for 2.5 minutes with May-Grunwald stain (Sigma), washed for 4 minutes in TBS, stained for 20-30 minutes with Giemsa stain (1:20 with ddH 2 0; Sigma) and briefly rinsed with ddH 2 0. Stained slides were dried overnight and cell types were identified using light microscopy. Approximately 100-200 cells were counted per slide and 3 slides were counted per mouse.
  • 405-ML is biologically active, con- tains no HIS-tag, is expressed in the bacculovirus Sf21 system, is also very pure (97 %), and can be purchased free of carrier-protein (BSA) .
  • BSA carrier-protein
  • a competitive ELISA was set up. This ELISA tests the ability of the different antisera to inhibit the interaction between soluble native murine IL5 and monoclonal antibodies TRFK4 or TRFK5, which are both neutralizing antibodies. Dilution series of antiserum pools were preincubated with soluble native mIL5 and the samples were added to ELISA plates coated with catching antibody TRFK5. Bound murine IL5 (which was not absorbed by the antisera) was next visualised using layers of biotinylated TRFK4 and subsequently horseradish peroxidase labeled streptavidin .
  • mIL5 specific autoantibodies are induced in mice immunized with either the HIS-mIL5wt or the HIS-mIL5.1 protein preparations (in 100% of the mice tested) .
  • B cell tolerance to mIL5 can be broken using recombinant HIS-tagged versions of both wild type and AutoVac murine IL5.
  • a plausible explanation for the observation that B cell tolerance is broken to the wild type protein is that the HIS-tag in these mice functions as a "foreign" immunogenic T helper epitope.
  • Another explanation could be that the administration of Complete Freund's Adjuvant breaks B cell tolerance to mIL5.
  • ELISA experiments were set up in order to determine whether antibodies specific for the inserted T helper epitope could be detected in sera from mIL5 protein immunised mice.
  • antisera bleed 2
  • Anti-HIS-mIL5.1 antiserum contained reactivity against the inserted P2 peptide, whereas neither anti-HIS-mIL5wt or anti-PBS/CFA reacted with the peptide.
  • the anti-HIS-mlLwt and anti- HIS-mIL5.1 antisera contained reactivity against the 15-mer HIS-tag (UNIZYME HIS-tag, SEQ ID NO: 25) that is fused to the N-terminal of both the wild type and AutoVac mIL5 proteins.
  • the peptide was synthesized and covalently immobilized in AquaBind microtiter plates, and pooled antisera from each immunization group (bleeds 1, 2 and 3) were tested for reactivity against the bound peptide. Antisera from all protein im- munized mice reacted with the synthetic HIS-tag peptide.
  • mice To determine if the anti-IL5 antibodies in vaccinated mice could down-regulate the in vi vo activity of IL5, we induced IL5-dependent eosinophilia in the lungs of the vaccinated mice. Eosinophils were induced by challenging sensitized mice with OVA mtranasally. High numbers of eosinophils were induced in control OVA mice and mice vaccinated with UniHis- mIL5.1, but not in Uni-His-mIL5 or PBS vaccinated mice.

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NO20015021L (no) 2001-12-21
NO20015021D0 (no) 2001-10-15
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AU4100800A (en) 2000-11-10
EE200100552A (et) 2002-12-16
KR20020084841A (ko) 2002-11-11
SK14832001A3 (sk) 2003-02-04
MXPA01010625A (es) 2003-09-04
WO2000065058A1 (en) 2000-11-02
PL351986A1 (en) 2003-07-14
HRP20010824A2 (en) 2002-12-31
US6746669B1 (en) 2004-06-08
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AU777952B2 (en) 2004-11-04
HUP0200958A3 (en) 2004-11-29
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CN1355846A (zh) 2002-06-26

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